Canonical Allele Identifier: CA1753246338

Gene: XRCC2

Linked Data

• dbSNP Id: rs2098026963

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152648406_152648407del , CM000669.2:g.152648406_152648407del	GRCh38
NC_000007.13:g.152345491_152345492del , CM000669.1:g.152345491_152345492del	GRCh37
NC_000007.12:g.151976424_151976425del	NCBI36
NG_027988.1:g.32759_32760del
NG_027988.2:g.32759_32760del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698506.1:c.*235_*236del	ENSP00000513758.1:n.*235_*236del
ENST00000359321.2:c.*235_*236del MANE Select	ENSP00000352271.1:n.*235_*236del
ENST00000359321.1:c.*235_*236del	ENSP00000352271.1:n.*235_*236del
ENST00000495707.1:n.1100_1101del
NM_005431.1:c.*235_*236del	NP_005422.1:n.*235_*236del
NM_005431.2:c.*235_*236del MANE Select	NP_005422.1:n.*235_*236del