Canonical Allele Identifier: CA1327724099
Gene: XRCC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216205570T= , CM000664.2:g.216205570T= GRCh38
NC_000002.11:g.217070293T= , CM000664.1:g.217070293T= GRCh37
NC_000002.10:g.216778538T= NCBI36
NG_029780.1:g.101274T=

Transcript Alleles

HGVS Amino-acid change
ENST00000392132.7:c.*368T= MANE Select ENSP00000375977.2:n.*368T=
ENST00000392132.6:c.*368T= ENSP00000375977.2:n.*368T=
ENST00000392133.7:c.*368T= ENSP00000375978.3:n.*368T=
NM_021141.3:c.*368T= NP_066964.1:n.*368T=
NM_021141.4:c.*368T= MANE Select NP_066964.1:n.*368T=