Canonical Allele Identifier: CA401215156

Gene: BIRC5

Linked Data

• MyVariant Identifiers: chr17:g.76219632T>G (hg19) ; chr17:g.78223551T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223551T>G , CM000679.2:g.78223551T>G	GRCh38
NC_000017.10:g.76219632T>G , CM000679.1:g.76219632T>G	GRCh37
NC_000017.9:g.73731227T>G	NCBI36
NG_029069.1:g.14356T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.426T>G MANE Select	ENSP00000324180.4:p.Asp142Glu
ENST00000301633.8:c.495T>G	ENSP00000301633.3:p.Asp165Glu
ENST00000350051.7:c.426T>G	ENSP00000324180.4:p.Asp142Glu
ENST00000374948.6:c.308T>G	ENSP00000364086.1:p.Ile103Ser
ENST00000589892.1:n.442T>G
ENST00000590925.6:c.*228T>G	ENSP00000467336.1:n.*228T>G
NM_001012270.1:c.308T>G	NP_001012270.1:p.Ile103Ser
NM_001012271.1:c.495T>G	NP_001012271.1:p.Asp165Glu
NM_001168.2:c.426T>G	NP_001159.2:p.Asp142Glu
XR_243654.3:n.628T>G
XR_934452.1:n.697T>G
XR_243654.5:n.628T>G
XR_934452.3:n.697T>G
NM_001168.3:c.426T>G MANE Select	NP_001159.2:p.Asp142Glu
NM_001012270.2:c.308T>G	NP_001012270.1:p.Ile103Ser
NM_001012271.2:c.495T>G	NP_001012271.1:p.Asp165Glu