Canonical Allele Identifier: CA401215215

Gene: BIRC5

Linked Data

• MyVariant Identifiers: chr17:g.76219638C>A (hg19) ; chr17:g.78223557C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223557C>A , CM000679.2:g.78223557C>A	GRCh38
NC_000017.10:g.76219638C>A , CM000679.1:g.76219638C>A	GRCh37
NC_000017.9:g.73731233C>A	NCBI36
NG_029069.1:g.14362C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*3C>A MANE Select	ENSP00000324180.4:n.*3C>A
ENST00000301633.8:c.*3C>A	ENSP00000301633.3:n.*3C>A
ENST00000350051.7:c.*3C>A	ENSP00000324180.4:n.*3C>A
ENST00000374948.6:c.314C>A	ENSP00000364086.1:p.Ala105Asp
ENST00000589892.1:n.448C>A
NM_001012270.1:c.314C>A	NP_001012270.1:p.Ala105Asp
NM_001012271.1:c.*3C>A	NP_001012271.1:n.*3C>A
NM_001168.2:c.*3C>A	NP_001159.2:n.*3C>A
XR_243654.3:n.634C>A
XR_934452.1:n.703C>A
XR_243654.5:n.634C>A
XR_934452.3:n.703C>A
NM_001168.3:c.*3C>A MANE Select	NP_001159.2:n.*3C>A
NM_001012270.2:c.314C>A	NP_001012270.1:p.Ala105Asp
NM_001012271.2:c.*3C>A	NP_001012271.1:n.*3C>A