Canonical Allele Identifier: CA294307123

Gene: BIRC5

Linked Data

• dbSNP Id: rs922951036
• MyVariant Identifiers: chr17:g.76219780C>T (hg19) ; chr17:g.78223699C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223699C>T , CM000679.2:g.78223699C>T	GRCh38
NC_000017.10:g.76219780C>T , CM000679.1:g.76219780C>T	GRCh37
NC_000017.9:g.73731375C>T	NCBI36
NG_029069.1:g.14504C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*145C>T MANE Select	ENSP00000324180.4:n.*145C>T
ENST00000301633.8:c.*145C>T	ENSP00000301633.3:n.*145C>T
ENST00000350051.7:c.*145C>T	ENSP00000324180.4:n.*145C>T
ENST00000374948.6:c.*42C>T	ENSP00000364086.1:n.*42C>T
ENST00000589892.1:n.590C>T
NM_001012270.1:c.*42C>T	NP_001012270.1:n.*42C>T
NM_001012271.1:c.*145C>T	NP_001012271.1:n.*145C>T
NM_001168.2:c.*145C>T	NP_001159.2:n.*145C>T
XR_243654.3:n.776C>T
XR_934452.1:n.845C>T
XR_243654.5:n.776C>T
XR_934452.3:n.845C>T
NM_001168.3:c.*145C>T MANE Select	NP_001159.2:n.*145C>T
NM_001012270.2:c.*42C>T	NP_001012270.1:n.*42C>T
NM_001012271.2:c.*145C>T	NP_001012271.1:n.*145C>T