Canonical Allele Identifier: CA645559668
Gene: XRCC2 HGNC NCBI

Linked Data

COSMIC: COSM166273
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152649134_152649135insT , CM000669.2:g.152649134_152649135insT GRCh38
NC_000007.13:g.152346219_152346220insT , CM000669.1:g.152346219_152346220insT GRCh37
NC_000007.12:g.151977152_151977153insT NCBI36
NG_027988.1:g.32031_32032insA
NG_027988.2:g.32031_32032insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.182_183insA ENSP00000513758.1:p.Val62GlyfsTer5
ENST00000359321.2:c.350_351insA MANE Select ENSP00000352271.1:p.Val118GlyfsTer5
ENST00000359321.1:c.350_351insA ENSP00000352271.1:p.Val118GlyfsTer5
ENST00000495707.1:n.372_373insA
NM_005431.1:c.350_351insA NP_005422.1:p.Val118GlyfsTer5
NM_005431.2:c.350_351insA MANE Select NP_005422.1:p.Val118GlyfsTer5
Search 100 bp 5'
Search 100 bp 3'