Canonical Allele Identifier: CA1753246342
Gene: XRCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648411_152648413delinsAAG , CM000669.2:g.152648411_152648413delinsAAG GRCh38
NC_000007.13:g.152345496_152345498delinsAAG , CM000669.1:g.152345496_152345498delinsAAG GRCh37
NC_000007.12:g.151976429_151976431delinsAAG NCBI36
NG_027988.1:g.32753_32755delinsCTT
NG_027988.2:g.32753_32755delinsCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.*229_*231delinsCTT ENSP00000513758.1:n.*229_*231delinsCTT
ENST00000359321.2:c.*229_*231delinsCTT MANE Select ENSP00000352271.1:n.*229_*231delinsCTT
ENST00000359321.1:c.*229_*231delinsCTT ENSP00000352271.1:n.*229_*231delinsCTT
ENST00000495707.1:n.1094_1096delinsCTT
NM_005431.1:c.*229_*231delinsCTT NP_005422.1:n.*229_*231delinsCTT
NM_005431.2:c.*229_*231delinsCTT MANE Select NP_005422.1:n.*229_*231delinsCTT