Canonical Allele Identifier: CA10584278
Gene: XRCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 246464
ClinVar RCV Id: RCV000235706
dbSNP Id: rs879254270
MyVariant Identifiers: chr7:g.152346000del (hg19) chr7:g.152648915del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648916del , CM000669.2:g.152648916del GRCh38
NC_000007.13:g.152346001del , CM000669.1:g.152346001del GRCh37
NC_000007.12:g.151976934del NCBI36
NG_027988.1:g.32251del
NG_027988.2:g.32251del

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.402del ENSP00000513758.1:p.Leu135PhefsTer8
ENST00000359321.2:c.570del MANE Select ENSP00000352271.1:p.Leu191PhefsTer8
ENST00000359321.1:c.570del ENSP00000352271.1:p.Leu191PhefsTer8
ENST00000495707.1:n.592del
NM_005431.1:c.570del NP_005422.1:p.Leu191PhefsTer8
NM_005431.2:c.570del MANE Select NP_005422.1:p.Leu191PhefsTer8
Search 100 bp 5'
Search 100 bp 3'