Canonical Allele Identifier: CA2685735559

Gene: XRCC2

Linked Data

• gnomAD v4: 7-152648434-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152648438del , CM000669.2:g.152648438del	GRCh38
NC_000007.13:g.152345523del , CM000669.1:g.152345523del	GRCh37
NC_000007.12:g.151976456del	NCBI36
NG_027988.1:g.32731del
NG_027988.2:g.32731del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698506.1:c.*207del	ENSP00000513758.1:n.*207del
ENST00000359321.2:c.*207del MANE Select	ENSP00000352271.1:n.*207del
ENST00000359321.1:c.*207del	ENSP00000352271.1:n.*207del
ENST00000495707.1:n.1072del
NM_005431.1:c.*207del	NP_005422.1:n.*207del
NM_005431.2:c.*207del MANE Select	NP_005422.1:n.*207del