Canonical Allele Identifier: CA1042299453
Gene: XRCC5 HGNC NCBI

Linked Data

dbSNP Id: rs1689927907

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216205561A>C , CM000664.2:g.216205561A>C GRCh38
NC_000002.11:g.217070284A>C , CM000664.1:g.217070284A>C GRCh37
NC_000002.10:g.216778529A>C NCBI36
NG_029780.1:g.101265A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000392132.7:c.*359A>C MANE Select ENSP00000375977.2:n.*359A>C
ENST00000392132.6:c.*359A>C ENSP00000375977.2:n.*359A>C
ENST00000392133.7:c.*359A>C ENSP00000375978.3:n.*359A>C
NM_021141.3:c.*359A>C NP_066964.1:n.*359A>C
NM_021141.4:c.*359A>C MANE Select NP_066964.1:n.*359A>C