Human (GRCh38.p14)
Description

GTF2H2 family member C [Source:HGNC Symbol;Acc:HGNC:31394]

Location

Chromosome 5: 69,560,191-69,595,221 forward strand.

GRCh38:CM000667.2

About this gene

This gene has 15 transcripts (splice variants), 207 orthologues and 1 paralogue.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000380729.8GTF2H2C-2014555395aaENSP00000370105.3
 
Protein coding
CCDS43325Q6P1K8 NM_001376000.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000510979.5GTF2H2C-2102952395aaENSP00000422907.1
 
Protein coding
CCDS43325Q6P1K8 -GENCODE basicAPPRIS P1TSL:1
ENST00000512736.5GTF2H2C-212832165aaENSP00000427224.1
 
Protein coding
D6RJD3 -GENCODE basicTSL:1
ENST00000507595.1GTF2H2C-208772253aaENSP00000427456.1
 
Protein coding
D6RID8 -TSL:5CDS 3' incomplete
ENST00000514162.5GTF2H2C-215610123aaENSP00000421312.1
 
Protein coding
D6RGC9 -GENCODE basicTSL:5
ENST00000446221.6GTF2H2C-202195651aaENSP00000403328.2
 
Nonsense mediated decay
D6RAW1 -TSL:1
ENST00000511629.6GTF2H2C-211187251aaENSP00000427486.1
 
Nonsense mediated decay
D6RAW1 -TSL:1
ENST00000506129.5GTF2H2C-20776992aaENSP00000427393.1
 
Nonsense mediated decay
D6RIT7 -TSL:5
ENST00000514069.6GTF2H2C-21458351aaENSP00000426434.2
 
Nonsense mediated decay
D6RAW1 -TSL:5
ENST00000513959.2GTF2H2C-213713No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000505737.2GTF2H2C-206475No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000503604.1GTF2H2C-2051176No protein-
 
Retained intron
--TSL:5
ENST00000502619.5GTF2H2C-2041106No protein-
 
Retained intron
--TSL:2
ENST00000508325.5GTF2H2C-209572No protein-
 
Retained intron
--TSL:3
ENST00000502599.1GTF2H2C-203412No protein-
 
Retained intron
--TSL:2