Canonical Allele Identifier: CA628014628
Gene: BIRC5 HGNC NCBI

Linked Data

gnomAD v2: 17-76219692-TC-T
MyVariant Identifiers: chr17:g.76219693del (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78223614del , CM000679.2:g.78223614del GRCh38
NC_000017.10:g.76219695del , CM000679.1:g.76219695del GRCh37
NC_000017.9:g.73731290del NCBI36
NG_029069.1:g.14419del

Transcript Alleles

HGVS Amino-acid change
ENST00000350051.8:c.*60del MANE Select ENSP00000324180.4:n.*60del
ENST00000301633.8:c.*60del ENSP00000301633.3:n.*60del
ENST00000350051.7:c.*60del ENSP00000324180.4:n.*60del
ENST00000374948.6:c.371del ENSP00000364086.1:p.Pro124LeufsTer11
ENST00000589892.1:n.505del
NM_001012270.1:c.371del NP_001012270.1:p.Pro124LeufsTer11
NM_001012271.1:c.*60del NP_001012271.1:n.*60del
NM_001168.2:c.*60del NP_001159.2:n.*60del
XR_243654.3:n.691del
XR_934452.1:n.760del
XR_243654.5:n.691del
XR_934452.3:n.760del
NM_001168.3:c.*60del MANE Select NP_001159.2:n.*60del
NM_001012270.2:c.371del NP_001012270.1:p.Pro124LeufsTer11
NM_001012271.2:c.*60del NP_001012271.1:n.*60del
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