Canonical Allele Identifier: CA2685736276
Gene: XRCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152660580del , CM000669.2:g.152660580del GRCh38
NC_000007.13:g.152357665del , CM000669.1:g.152357665del GRCh37
NC_000007.12:g.151988598del NCBI36
NG_027988.1:g.20589del
NG_027988.2:g.20589del

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.-47-11214del ENSP00000513758.1:n.-47-11214del
ENST00000698507.1:n.313del
ENST00000359321.2:c.121+124del MANE Select ENSP00000352271.1:n.121+124del
ENST00000359321.1:c.121+124del ENSP00000352271.1:n.121+124del
ENST00000495707.1:n.143+124del
NM_005431.1:c.121+124del NP_005422.1:n.121+124del
NM_005431.2:c.121+124del MANE Select NP_005422.1:n.121+124del