Canonical Allele Identifier: CA401214952

Gene: BIRC5

Linked Data

• gnomAD v4: 17-78223528-A-G
• MyVariant Identifiers: chr17:g.76219609A>G (hg19) ; chr17:g.78223528A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223528A>G , CM000679.2:g.78223528A>G	GRCh38
NC_000017.10:g.76219609A>G , CM000679.1:g.76219609A>G	GRCh37
NC_000017.9:g.73731204A>G	NCBI36
NG_029069.1:g.14333A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.403A>G MANE Select	ENSP00000324180.4:p.Ile135Val
ENST00000301633.8:c.472A>G	ENSP00000301633.3:p.Ile158Val
ENST00000350051.7:c.403A>G	ENSP00000324180.4:p.Ile135Val
ENST00000374948.6:c.285A>G	ENSP00000364086.1:p.Pro95=
ENST00000589892.1:n.419A>G
ENST00000590925.6:c.*205A>G	ENSP00000467336.1:n.*205A>G
NM_001012270.1:c.285A>G	NP_001012270.1:p.Pro95=
NM_001012271.1:c.472A>G	NP_001012271.1:p.Ile158Val
NM_001168.2:c.403A>G	NP_001159.2:p.Ile135Val
XR_243654.3:n.605A>G
XR_934452.1:n.674A>G
XR_243654.5:n.605A>G
XR_934452.3:n.674A>G
NM_001168.3:c.403A>G MANE Select	NP_001159.2:p.Ile135Val
NM_001012270.2:c.285A>G	NP_001012270.1:p.Pro95=
NM_001012271.2:c.472A>G	NP_001012271.1:p.Ile158Val