Canonical Allele Identifier: CA502083072
Gene: BIRC5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.76219788T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78223707T>A , CM000679.2:g.78223707T>A GRCh38
NC_000017.10:g.76219788T>A , CM000679.1:g.76219788T>A GRCh37
NC_000017.9:g.73731383T>A NCBI36
NG_029069.1:g.14512T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000350051.8:c.*153T>A MANE Select ENSP00000324180.4:n.*153T>A
ENST00000301633.8:c.*153T>A ENSP00000301633.3:n.*153T>A
ENST00000350051.7:c.*153T>A ENSP00000324180.4:n.*153T>A
ENST00000374948.6:c.*50T>A ENSP00000364086.1:n.*50T>A
ENST00000589892.1:n.598T>A
NM_001012270.1:c.*50T>A NP_001012270.1:n.*50T>A
NM_001012271.1:c.*153T>A NP_001012271.1:n.*153T>A
NM_001168.2:c.*153T>A NP_001159.2:n.*153T>A
XR_243654.3:n.784T>A
XR_934452.1:n.853T>A
XR_243654.5:n.784T>A
XR_934452.3:n.853T>A
NM_001168.3:c.*153T>A MANE Select NP_001159.2:n.*153T>A
NM_001012270.2:c.*50T>A NP_001012270.1:n.*50T>A
NM_001012271.2:c.*153T>A NP_001012271.1:n.*153T>A
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