Canonical Allele Identifier: CA2685735523

Gene: XRCC2

Linked Data

• gnomAD v4: 7-152648412-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152648413dup , CM000669.2:g.152648413dup	GRCh38
NC_000007.13:g.152345498dup , CM000669.1:g.152345498dup	GRCh37
NC_000007.12:g.151976431dup	NCBI36
NG_027988.1:g.32753dup
NG_027988.2:g.32753dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698506.1:c.*229dup	ENSP00000513758.1:n.*229dup
ENST00000359321.2:c.*229dup MANE Select	ENSP00000352271.1:n.*229dup
ENST00000359321.1:c.*229dup	ENSP00000352271.1:n.*229dup
ENST00000495707.1:n.1094dup
NM_005431.1:c.*229dup	NP_005422.1:n.*229dup
NM_005431.2:c.*229dup MANE Select	NP_005422.1:n.*229dup