Human (GRCh38.p14)
Description

X-ray repair cross complementing 4 [Source:HGNC Symbol;Acc:HGNC:12831]

Location
About this transcript

This transcript has 8 exons, is annotated with 13 domains and features, is associated with 111664 variant alleles and maps to 468 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000396027.9XRCC4-2031602334aaENSP00000379344.4
 
Protein coding
CCDS4058Q13426-2 NM_003401.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS ALT1TSL:5
ENST00000282268.7XRCC4-2011696334aaENSP00000282268.3
 
Protein coding
CCDS4058Q13426-2 -GENCODE basicAPPRIS ALT1TSL:1
ENST00000511817.1XRCC4-2051636336aaENSP00000421491.1
 
Protein coding
CCDS4059Q13426-1 -GENCODE basicAPPRIS P3TSL:1
ENST00000338635.10XRCC4-2021579336aaENSP00000342011.6
 
Protein coding
CCDS4059Q13426-1 -GENCODE basicAPPRIS P3TSL:2
ENST00000509268.1XRCC4-2041567No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000542685.5XRCC4-2061243No protein-
 
Protein coding CDS not defined
--TSL:1
Statistics

Exons: 8, Coding exons: 7, Transcript length: 1,602 bps, Translation length: 334 residues

MANE

This MANE Select transcript contains ENSP00000379344 and matches to NM_003401.5 and NP_003392.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q13426

CCDS

This transcript is a member of the Human CCDS set: CCDS4058

Transcript Support Level (TSL)

TSL:5

Version

ENST00000396027.9

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

GENCODE basic gene

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