Canonical Allele Identifier: CA2663022306
Gene: XRCC5 HGNC NCBI

Linked Data

gnomAD v4: 2-216122035-C-CT
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216122036dup , CM000664.2:g.216122036dup GRCh38
NC_000002.11:g.216986759dup , CM000664.1:g.216986759dup GRCh37
NC_000002.10:g.216695004dup NCBI36
NG_029780.1:g.17740dup

Transcript Alleles

HGVS Amino-acid change
ENST00000392132.7:c.492-26dup MANE Select ENSP00000375977.2:n.492-26dup
ENST00000392132.6:c.492-26dup ENSP00000375977.2:n.492-26dup
ENST00000392133.7:c.492-26dup ENSP00000375978.3:n.492-26dup
ENST00000460284.5:n.1034-26dup
NM_021141.3:c.492-26dup NP_066964.1:n.492-26dup
NM_021141.4:c.492-26dup MANE Select NP_066964.1:n.492-26dup
Search 100 bp 5'
Search 100 bp 3'