Human (GRCh38.p14)
Description

X-ray repair cross complementing 1 [Source:HGNC Symbol;Acc:HGNC:12828]

Gene Synonyms

RCC

Location

Chromosome 19: 43,543,311-43,580,473 reverse strand.

GRCh38:CM000681.2

About this gene

This gene has 9 transcripts (splice variants), 189 orthologues, 1 paralogue and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000262887.10XRCC1-2012052633aaENSP00000262887.5
 
Protein coding
CCDS12624P18887 NM_006297.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000543982.5XRCC1-2021994602aaENSP00000443671.1
 
Protein coding
F5H8D7 -GENCODE basicTSL:2
ENST00000598165.5XRCC1-207913292aaENSP00000470045.1
 
Protein coding
M0QYS5 -TSL:3CDS 3' incomplete
ENST00000599693.5XRCC1-209628210aaENSP00000472128.1
 
Protein coding
M0R1U8 -TSL:3CDS 5' and 3' incomplete
ENST00000594107.1XRCC1-203586172aaENSP00000471159.1
 
Protein coding
M0R0D2 -TSL:2CDS 3' incomplete
ENST00000597811.5XRCC1-206809165aaENSP00000470391.1
 
Nonsense mediated decay
M0QZ96 -TSL:5CDS 5' incomplete
ENST00000595789.5XRCC1-2051147No protein-
 
Retained intron
--TSL:3
ENST00000598422.1XRCC1-208701No protein-
 
Retained intron
--TSL:2
ENST00000594511.1XRCC1-204571No protein-
 
Retained intron
--TSL:4