Canonical Allele Identifier: CA764677210
Gene: XRCC5 HGNC NCBI

Linked Data

dbSNP Id: rs1190304303
gnomAD v3: 2-216205568-CAT-C
gnomAD v4: 2-216205568-CAT-C
MyVariant Identifiers: chr2:g.217070292_217070293del (hg19) chr2:g.216205569_216205570del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216205569_216205570del , CM000664.2:g.216205569_216205570del GRCh38
NC_000002.11:g.217070292_217070293del , CM000664.1:g.217070292_217070293del GRCh37
NC_000002.10:g.216778537_216778538del NCBI36
NG_029780.1:g.101273_101274del

Transcript Alleles

HGVS Amino-acid change
ENST00000392132.7:c.*367_*368del MANE Select ENSP00000375977.2:n.*367_*368del
ENST00000392132.6:c.*367_*368del ENSP00000375977.2:n.*367_*368del
ENST00000392133.7:c.*367_*368del ENSP00000375978.3:n.*367_*368del
NM_021141.3:c.*367_*368del NP_066964.1:n.*367_*368del
NM_021141.4:c.*367_*368del MANE Select NP_066964.1:n.*367_*368del
Search 100 bp 5'
Search 100 bp 3'