Canonical Allele Identifier: CA2778474372
Gene: XRCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648838_152648839insACCAAACACACCCAACACA , CM000669.2:g.152648838_152648839insACCAAACACACCCAACACA GRCh38
NC_000007.13:g.152345923_152345924insACCAAACACACCCAACACA , CM000669.1:g.152345923_152345924insACCAAACACACCCAACACA GRCh37
NC_000007.12:g.151976856_151976857insACCAAACACACCCAACACA NCBI36
NG_027988.1:g.32332_32333insTGGGTGTGTTTGGTTGTGT
NG_027988.2:g.32332_32333insTGGGTGTGTTTGGTTGTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.483_484insTGGGTGTGTTTGGTTGTGT ENSP00000513758.1:p.Asp162TrpfsTer7
ENST00000359321.2:c.651_652insTGGGTGTGTTTGGTTGTGT MANE Select ENSP00000352271.1:p.Asp218TrpfsTer7
ENST00000359321.1:c.651_652insTGGGTGTGTTTGGTTGTGT ENSP00000352271.1:p.Asp218TrpfsTer7
ENST00000495707.1:n.673_674insTGGGTGTGTTTGGTTGTGT
NM_005431.1:c.651_652insTGGGTGTGTTTGGTTGTGT NP_005422.1:p.Asp218TrpfsTer7
NM_005431.2:c.651_652insTGGGTGTGTTTGGTTGTGT MANE Select NP_005422.1:p.Asp218TrpfsTer7