Canonical Allele Identifier: CA1108857364
Gene: XRCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648412dup , CM000669.2:g.152648412dup GRCh38
NC_000007.13:g.152345497dup , CM000669.1:g.152345497dup GRCh37
NC_000007.12:g.151976430dup NCBI36
NG_027988.1:g.32758dup
NG_027988.2:g.32758dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.*234dup ENSP00000513758.1:n.*234dup
ENST00000359321.2:c.*234dup MANE Select ENSP00000352271.1:n.*234dup
ENST00000359321.1:c.*234dup ENSP00000352271.1:n.*234dup
ENST00000495707.1:n.1099dup
NM_005431.1:c.*234dup NP_005422.1:n.*234dup
NM_005431.2:c.*234dup MANE Select NP_005422.1:n.*234dup