Canonical Allele Identifier: CA2573049660
Gene: XRCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648413_152648415delinsGAA , CM000669.2:g.152648413_152648415delinsGAA GRCh38
NC_000007.13:g.152345498_152345500delinsGAA , CM000669.1:g.152345498_152345500delinsGAA GRCh37
NC_000007.12:g.151976431_151976433delinsGAA NCBI36
NG_027988.1:g.32751_32753delinsTTC
NG_027988.2:g.32751_32753delinsTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.*227_*229delinsTTC ENSP00000513758.1:n.*227_*229delinsTTC
ENST00000359321.2:c.*227_*229delinsTTC MANE Select ENSP00000352271.1:n.*227_*229delinsTTC
ENST00000359321.1:c.*227_*229delinsTTC ENSP00000352271.1:n.*227_*229delinsTTC
ENST00000495707.1:n.1092_1094delinsTTC
NM_005431.1:c.*227_*229delinsTTC NP_005422.1:n.*227_*229delinsTTC
NM_005431.2:c.*227_*229delinsTTC MANE Select NP_005422.1:n.*227_*229delinsTTC