Canonical Allele Identifier: CA1327685986
Gene: XRCC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216122113C= , CM000664.2:g.216122113C= GRCh38
NC_000002.11:g.216986836C= , CM000664.1:g.216986836C= GRCh37
NC_000002.10:g.216695081C= NCBI36
NG_029780.1:g.17817C=

Transcript Alleles

HGVS Amino-acid change
ENST00000392132.7:c.543C= MANE Select ENSP00000375977.2:p.Gly181=
ENST00000392132.6:c.543C= ENSP00000375977.2:p.Gly181=
ENST00000392133.7:c.543C= ENSP00000375978.3:p.Gly181=
ENST00000460284.5:n.1085C=
NM_021141.3:c.543C= NP_066964.1:p.Gly181=
NM_021141.4:c.543C= MANE Select NP_066964.1:p.Gly181=