Canonical Allele Identifier: CA401215849

Gene: BIRC5

Linked Data

• MyVariant Identifiers: chr17:g.76219725T>G (hg19) ; chr17:g.78223644T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223644T>G , CM000679.2:g.78223644T>G	GRCh38
NC_000017.10:g.76219725T>G , CM000679.1:g.76219725T>G	GRCh37
NC_000017.9:g.73731320T>G	NCBI36
NG_029069.1:g.14449T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*90T>G MANE Select	ENSP00000324180.4:n.*90T>G
ENST00000301633.8:c.*90T>G	ENSP00000301633.3:n.*90T>G
ENST00000350051.7:c.*90T>G	ENSP00000324180.4:n.*90T>G
ENST00000374948.6:c.401T>G	ENSP00000364086.1:p.Leu134Ter
ENST00000589892.1:n.535T>G
NM_001012270.1:c.401T>G	NP_001012270.1:p.Leu134Ter
NM_001012271.1:c.*90T>G	NP_001012271.1:n.*90T>G
NM_001168.2:c.*90T>G	NP_001159.2:n.*90T>G
XR_243654.3:n.721T>G
XR_934452.1:n.790T>G
XR_243654.5:n.721T>G
XR_934452.3:n.790T>G
NM_001168.3:c.*90T>G MANE Select	NP_001159.2:n.*90T>G
NM_001012270.2:c.401T>G	NP_001012270.1:p.Leu134Ter
NM_001012271.2:c.*90T>G	NP_001012271.1:n.*90T>G