Canonical Allele Identifier: CA502083060

Gene: BIRC5

Linked Data

• MyVariant Identifiers: chr17:g.76219787T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223706T>A , CM000679.2:g.78223706T>A	GRCh38
NC_000017.10:g.76219787T>A , CM000679.1:g.76219787T>A	GRCh37
NC_000017.9:g.73731382T>A	NCBI36
NG_029069.1:g.14511T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350051.8:c.*152T>A MANE Select	ENSP00000324180.4:n.*152T>A
ENST00000301633.8:c.*152T>A	ENSP00000301633.3:n.*152T>A
ENST00000350051.7:c.*152T>A	ENSP00000324180.4:n.*152T>A
ENST00000374948.6:c.*49T>A	ENSP00000364086.1:n.*49T>A
ENST00000589892.1:n.597T>A
NM_001012270.1:c.*49T>A	NP_001012270.1:n.*49T>A
NM_001012271.1:c.*152T>A	NP_001012271.1:n.*152T>A
NM_001168.2:c.*152T>A	NP_001159.2:n.*152T>A
XR_243654.3:n.783T>A
XR_934452.1:n.852T>A
XR_243654.5:n.783T>A
XR_934452.3:n.852T>A
NM_001168.3:c.*152T>A MANE Select	NP_001159.2:n.*152T>A
NM_001012270.2:c.*49T>A	NP_001012270.1:n.*49T>A
NM_001012271.2:c.*152T>A	NP_001012271.1:n.*152T>A