Canonical Allele Identifier: CA1753257396
Gene: XRCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152660793_152660795delinsAAG , CM000669.2:g.152660793_152660795delinsAAG GRCh38
NC_000007.13:g.152357878_152357880delinsAAG , CM000669.1:g.152357878_152357880delinsAAG GRCh37
NC_000007.12:g.151988811_151988813delinsAAG NCBI36
NG_027988.1:g.20371_20373delinsCTT
NG_027988.2:g.20371_20373delinsCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-47-11432_-47-11430delinsCTT ENSP00000513758.1:n.-47-11432_-47-11430delinsCTT
ENST00000698507.1:n.108-13_108-11delinsCTT
ENST00000359321.2:c.40-13_40-11delinsCTT MANE Select ENSP00000352271.1:n.40-13_40-11delinsCTT
ENST00000359321.1:c.40-13_40-11delinsCTT ENSP00000352271.1:n.40-13_40-11delinsCTT
ENST00000495707.1:n.62-13_62-11delinsCTT
NM_005431.1:c.40-13_40-11delinsCTT NP_005422.1:n.40-13_40-11delinsCTT
NM_005431.2:c.40-13_40-11delinsCTT MANE Select NP_005422.1:n.40-13_40-11delinsCTT