Canonical Allele Identifier: CA651996991

Gene: XRCC2

Linked Data

• COSMIC: COSN19069937

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152648415_152648416insG , CM000669.2:g.152648415_152648416insG	GRCh38
NC_000007.13:g.152345500_152345501insG , CM000669.1:g.152345500_152345501insG	GRCh37
NC_000007.12:g.151976433_151976434insG	NCBI36
NG_027988.1:g.32750_32751insC
NG_027988.2:g.32750_32751insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698506.1:c.*226_*227insC	ENSP00000513758.1:n.*226_*227insC
ENST00000359321.2:c.*226_*227insC MANE Select	ENSP00000352271.1:n.*226_*227insC
ENST00000359321.1:c.*226_*227insC	ENSP00000352271.1:n.*226_*227insC
ENST00000495707.1:n.1091_1092insC
NM_005431.1:c.*226_*227insC	NP_005422.1:n.*226_*227insC
NM_005431.2:c.*226_*227insC MANE Select	NP_005422.1:n.*226_*227insC