Canonical Allele Identifier: CA401215256

Gene: BIRC5

Linked Data

• MyVariant Identifiers: chr17:g.76219647G>C (hg19) ; chr17:g.78223566G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223566G>C , CM000679.2:g.78223566G>C	GRCh38
NC_000017.10:g.76219647G>C , CM000679.1:g.76219647G>C	GRCh37
NC_000017.9:g.73731242G>C	NCBI36
NG_029069.1:g.14371G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*12G>C MANE Select	ENSP00000324180.4:n.*12G>C
ENST00000301633.8:c.*12G>C	ENSP00000301633.3:n.*12G>C
ENST00000350051.7:c.*12G>C	ENSP00000324180.4:n.*12G>C
ENST00000374948.6:c.323G>C	ENSP00000364086.1:p.Arg108Pro
ENST00000589892.1:n.457G>C
NM_001012270.1:c.323G>C	NP_001012270.1:p.Arg108Pro
NM_001012271.1:c.*12G>C	NP_001012271.1:n.*12G>C
NM_001168.2:c.*12G>C	NP_001159.2:n.*12G>C
XR_243654.3:n.643G>C
XR_934452.1:n.712G>C
XR_243654.5:n.643G>C
XR_934452.3:n.712G>C
NM_001168.3:c.*12G>C MANE Select	NP_001159.2:n.*12G>C
NM_001012270.2:c.323G>C	NP_001012270.1:p.Arg108Pro
NM_001012271.2:c.*12G>C	NP_001012271.1:n.*12G>C