Human (GRCh38.p14)
Description

solute carrier family 25 member 26 [Source:HGNC Symbol;Acc:HGNC:20661]

Gene Synonyms

SAMC

Location

Scaffold HG2235_PATCH: 110,410-365,012 forward strand.

GRCh38:KQ031385.1

View this gene on the primary assembly.

About this gene

This gene has 6 transcripts (splice variants), 1 gene allele and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000633701.1SLC25A26-2272673274aaENSP00000488659.1
 
Protein coding
Q70HW3-1 -Ensembl CanonicalGENCODE basic
ENST00000633238.1SLC25A26-2251096210aaENSP00000487996.1
 
Protein coding
H7C430 -GENCODE basic
ENST00000632575.1SLC25A26-2231023186aaENSP00000488865.1
 
Protein coding
Q70HW3-2 -GENCODE basic
ENST00000634032.1SLC25A26-228387986aaENSP00000487656.1
 
Nonsense mediated decay
H0YCZ5 --
ENST00000632740.1SLC25A26-224184091aaENSP00000487788.1
 
Nonsense mediated decay
H0YF50 -CDS 5' incomplete
ENST00000633644.1SLC25A26-226375No protein-
 
Protein coding CDS not defined
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