Canonical Allele Identifier: CA294307023

Gene: BIRC5

Linked Data

• dbSNP Id: rs561843820
• gnomAD v3: 17-78223582-A-G
• gnomAD v4: 17-78223582-A-G
• MyVariant Identifiers: chr17:g.76219663A>G (hg19) ; chr17:g.78223582A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223582A>G , CM000679.2:g.78223582A>G	GRCh38
NC_000017.10:g.76219663A>G , CM000679.1:g.76219663A>G	GRCh37
NC_000017.9:g.73731258A>G	NCBI36
NG_029069.1:g.14387A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*28A>G MANE Select	ENSP00000324180.4:n.*28A>G
ENST00000301633.8:c.*28A>G	ENSP00000301633.3:n.*28A>G
ENST00000350051.7:c.*28A>G	ENSP00000324180.4:n.*28A>G
ENST00000374948.6:c.339A>G	ENSP00000364086.1:p.Pro113=
ENST00000589892.1:n.473A>G
NM_001012270.1:c.339A>G	NP_001012270.1:p.Pro113=
NM_001012271.1:c.*28A>G	NP_001012271.1:n.*28A>G
NM_001168.2:c.*28A>G	NP_001159.2:n.*28A>G
XR_243654.3:n.659A>G
XR_934452.1:n.728A>G
XR_243654.5:n.659A>G
XR_934452.3:n.728A>G
NM_001168.3:c.*28A>G MANE Select	NP_001159.2:n.*28A>G
NM_001012270.2:c.339A>G	NP_001012270.1:p.Pro113=
NM_001012271.2:c.*28A>G	NP_001012271.1:n.*28A>G