Canonical Allele Identifier: CA2838812125
Gene: XRCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152675984dup , CM000669.2:g.152675984dup GRCh38
NC_000007.13:g.152373069dup , CM000669.1:g.152373069dup GRCh37
NC_000007.12:g.152004002dup NCBI36
NG_027988.1:g.5185dup
NG_027988.2:g.5185dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-48+60dup ENSP00000513758.1:n.-48+60dup
ENST00000698507.1:n.107+60dup
ENST00000359321.2:c.39+60dup MANE Select ENSP00000352271.1:n.39+60dup
ENST00000359321.1:c.39+60dup ENSP00000352271.1:n.39+60dup
NM_005431.1:c.39+60dup NP_005422.1:n.39+60dup
NM_005431.2:c.39+60dup MANE Select NP_005422.1:n.39+60dup