Canonical Allele Identifier: CA16612057
Gene: XRCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 409961
ClinVar RCV Id: RCV001297351
dbSNP Id: rs1060502667
MyVariant Identifiers: chr7:g.152345780_152345781del (hg19) chr7:g.152648695_152648696del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648696_152648697del , CM000669.2:g.152648696_152648697del GRCh38
NC_000007.13:g.152345781_152345782del , CM000669.1:g.152345781_152345782del GRCh37
NC_000007.12:g.151976714_151976715del NCBI36
NG_027988.1:g.32470_32471del
NG_027988.2:g.32470_32471del

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.621_622del ENSP00000513758.1:p.Asn207LysfsTer15
ENST00000359321.2:c.789_790del MANE Select ENSP00000352271.1:p.Asn263LysfsTer15
ENST00000359321.1:c.789_790del ENSP00000352271.1:p.Asn263LysfsTer15
ENST00000495707.1:n.811_812del
NM_005431.1:c.789_790del NP_005422.1:p.Asn263LysfsTer15
NM_005431.2:c.789_790del MANE Select NP_005422.1:p.Asn263LysfsTer15
Search 100 bp 5'
Search 100 bp 3'