Canonical Allele Identifier: CA502082386

Gene: BIRC5

Linked Data

• gnomAD v4: 17-78223659-A-T
• MyVariant Identifiers: chr17:g.76219740A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223659A>T , CM000679.2:g.78223659A>T	GRCh38
NC_000017.10:g.76219740A>T , CM000679.1:g.76219740A>T	GRCh37
NC_000017.9:g.73731335A>T	NCBI36
NG_029069.1:g.14464A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*105A>T MANE Select	ENSP00000324180.4:n.*105A>T
ENST00000301633.8:c.*105A>T	ENSP00000301633.3:n.*105A>T
ENST00000350051.7:c.*105A>T	ENSP00000324180.4:n.*105A>T
ENST00000374948.6:c.*2A>T	ENSP00000364086.1:n.*2A>T
ENST00000589892.1:n.550A>T
NM_001012270.1:c.*2A>T	NP_001012270.1:n.*2A>T
NM_001012271.1:c.*105A>T	NP_001012271.1:n.*105A>T
NM_001168.2:c.*105A>T	NP_001159.2:n.*105A>T
XR_243654.3:n.736A>T
XR_934452.1:n.805A>T
XR_243654.5:n.736A>T
XR_934452.3:n.805A>T
NM_001168.3:c.*105A>T MANE Select	NP_001159.2:n.*105A>T
NM_001012270.2:c.*2A>T	NP_001012270.1:n.*2A>T
NM_001012271.2:c.*105A>T	NP_001012271.1:n.*105A>T