Canonical Allele Identifier: CA1108857338
Gene: XRCC2 HGNC NCBI

Linked Data

gnomAD v3: 7-152648402-TG-T
gnomAD v4: 7-152648402-TG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648403del , CM000669.2:g.152648403del GRCh38
NC_000007.13:g.152345488del , CM000669.1:g.152345488del GRCh37
NC_000007.12:g.151976421del NCBI36
NG_027988.1:g.32763del
NG_027988.2:g.32763del

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.*239del ENSP00000513758.1:n.*239del
ENST00000359321.2:c.*239del MANE Select ENSP00000352271.1:n.*239del
ENST00000359321.1:c.*239del ENSP00000352271.1:n.*239del
ENST00000495707.1:n.1104del
NM_005431.1:c.*239del NP_005422.1:n.*239del
NM_005431.2:c.*239del MANE Select NP_005422.1:n.*239del
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