Human (GRCh38.p14)
Description

DNA cross-link repair 1B [Source:HGNC Symbol;Acc:HGNC:17641]

Gene Synonyms

APOLLO, FLJ12810, FLJ13998, SNM1B

About this transcript

This transcript has 4 exons, is annotated with 20 domains and features, is associated with 4530 variant alleles and maps to 418 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000650450.2DCLRE1B-2033755532aaENSP00000498042.1
 
Protein coding
CCDS866Q9H816 NM_022836.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1
ENST00000650596.1DCLRE1B-2041980471aaENSP00000497882.1
 
Protein coding
A0A3B3ITQ0 -GENCODE basic
ENST00000466480.2DCLRE1B-201319972aaENSP00000497696.1
 
Nonsense mediated decay
A0A3B3IT16 -TSL:1
ENST00000648795.1DCLRE1B-202196072aaENSP00000497557.1
 
Nonsense mediated decay
A0A3B3IT16 --
ENST00000697125.1DCLRE1B-205569No protein-
 
Protein coding CDS not defined
---
ENST00000697126.1DCLRE1B-2063872No protein-
 
Retained intron
---
Statistics

Exons: 4, Coding exons: 4, Transcript length: 3,755 bps, Translation length: 532 residues

MANE

This MANE Select transcript contains ENSP00000498042 and matches to NM_022836.4 and NP_073747.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9H816

CCDS

This transcript is a member of the Human CCDS set: CCDS866

Version

ENST00000650450.2

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.