Canonical Allele Identifier: CA401215024
Gene: BIRC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78223538T>G , CM000679.2:g.78223538T>G GRCh38
NC_000017.10:g.76219619T>G , CM000679.1:g.76219619T>G GRCh37
NC_000017.9:g.73731214T>G NCBI36
NG_029069.1:g.14343T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000350051.8:c.413T>G MANE Select ENSP00000324180.4:p.Leu138Arg
ENST00000301633.8:c.482T>G ENSP00000301633.3:p.Leu161Arg
ENST00000350051.7:c.413T>G ENSP00000324180.4:p.Leu138Arg
ENST00000374948.6:c.295T>G ENSP00000364086.1:p.Trp99Gly
ENST00000589892.1:n.429T>G
ENST00000590925.6:c.*215T>G ENSP00000467336.1:n.*215T>G
NM_001012270.1:c.295T>G NP_001012270.1:p.Trp99Gly
NM_001012271.1:c.482T>G NP_001012271.1:p.Leu161Arg
NM_001168.2:c.413T>G NP_001159.2:p.Leu138Arg
XR_243654.3:n.615T>G
XR_934452.1:n.684T>G
XR_243654.5:n.615T>G
XR_934452.3:n.684T>G
NM_001168.3:c.413T>G MANE Select NP_001159.2:p.Leu138Arg
NM_001012270.2:c.295T>G NP_001012270.1:p.Trp99Gly
NM_001012271.2:c.482T>G NP_001012271.1:p.Leu161Arg