Canonical Allele Identifier: CA1108867626

Gene: XRCC2

Linked Data

• gnomAD v3: 7-152675665-G-GAACAGGTGGTGTTTGCGGAGGTTGCCTCACCTC
• gnomAD v4: 7-152675665-G-GAACAGGTGGTGTTTGCGGAGGTTGCCTCACCTC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152675665_152675666insAACAGGTGGTGTTTGCGGAGGTTGCCTCACCTC , CM000669.2:g.152675665_152675666insAACAGGTGGTGTTTGCGGAGGTTGCCTCACCTC	GRCh38
NC_000007.13:g.152372750_152372751insAACAGGTGGTGTTTGCGGAGGTTGCCTCACCTC , CM000669.1:g.152372750_152372751insAACAGGTGGTGTTTGCGGAGGTTGCCTCACCTC	GRCh37
NC_000007.12:g.152003683_152003684insAACAGGTGGTGTTTGCGGAGGTTGCCTCACCTC	NCBI36
NG_027988.1:g.5500_5501insGAGGTGAGGCAACCTCCGCAAACACCACCTGTT
NG_027988.2:g.5500_5501insGAGGTGAGGCAACCTCCGCAAACACCACCTGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698506.1:c.-48+375_-48+376insGAGGTGAGGCAACCTCCGCAAACACCACCTGTT	ENSP00000513758.1:n.-48+375_-48+376insGAGGTGAGGCAACCTCCGCAAAC...
ENST00000698507.1:n.107+375_107+376insGAGGTGAGGCAACCTCCGCAAACACCACCTGTT
ENST00000359321.2:c.39+375_39+376insGAGGTGAGGCAACCTCCGCAAACACCACCTGTT MANE Select	ENSP00000352271.1:n.39+375_39+376insGAGGTGAGGCAACCTCCGCAAACAC...
ENST00000359321.1:c.39+375_39+376insGAGGTGAGGCAACCTCCGCAAACACCACCTGTT	ENSP00000352271.1:n.39+375_39+376insGAGGTGAGGCAACCTCCGCAAACAC...
NM_005431.1:c.39+375_39+376insGAGGTGAGGCAACCTCCGCAAACACCACCTGTT	NP_005422.1:n.39+375_39+376insGAGGTGAGGCAACCTCCGCAAACACCACCTG...
NM_005431.2:c.39+375_39+376insGAGGTGAGGCAACCTCCGCAAACACCACCTGTT MANE Select	NP_005422.1:n.39+375_39+376insGAGGTGAGGCAACCTCCGCAAACACCACCTG...