Canonical Allele Identifier: CA1108867621

Gene: XRCC2

Linked Data

• gnomAD v3: 7-152675570-CACG-C
• gnomAD v4: 7-152675570-CACG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152675571_152675573del , CM000669.2:g.152675571_152675573del	GRCh38
NC_000007.13:g.152372656_152372658del , CM000669.1:g.152372656_152372658del	GRCh37
NC_000007.12:g.152003589_152003591del	NCBI36
NG_027988.1:g.5593_5595del
NG_027988.2:g.5593_5595del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698506.1:c.-48+468_-48+470del	ENSP00000513758.1:n.-48+468_-48+470del
ENST00000698507.1:n.107+468_107+470del
ENST00000359321.2:c.39+468_39+470del MANE Select	ENSP00000352271.1:n.39+468_39+470del
ENST00000359321.1:c.39+468_39+470del	ENSP00000352271.1:n.39+468_39+470del
NM_005431.1:c.39+468_39+470del	NP_005422.1:n.39+468_39+470del
NM_005431.2:c.39+468_39+470del MANE Select	NP_005422.1:n.39+468_39+470del