Canonical Allele Identifier: CA401214942

Gene: BIRC5

Linked Data

• MyVariant Identifiers: chr17:g.76219608C>G (hg19) ; chr17:g.78223527C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223527C>G , CM000679.2:g.78223527C>G	GRCh38
NC_000017.10:g.76219608C>G , CM000679.1:g.76219608C>G	GRCh37
NC_000017.9:g.73731203C>G	NCBI36
NG_029069.1:g.14332C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.402C>G MANE Select	ENSP00000324180.4:p.Ala134=
ENST00000301633.8:c.471C>G	ENSP00000301633.3:p.Ala157=
ENST00000350051.7:c.402C>G	ENSP00000324180.4:p.Ala134=
ENST00000374948.6:c.284C>G	ENSP00000364086.1:p.Pro95Arg
ENST00000589892.1:n.418C>G
ENST00000590925.6:c.*204C>G	ENSP00000467336.1:n.*204C>G
NM_001012270.1:c.284C>G	NP_001012270.1:p.Pro95Arg
NM_001012271.1:c.471C>G	NP_001012271.1:p.Ala157=
NM_001168.2:c.402C>G	NP_001159.2:p.Ala134=
XR_243654.3:n.604C>G
XR_934452.1:n.673C>G
XR_243654.5:n.604C>G
XR_934452.3:n.673C>G
NM_001168.3:c.402C>G MANE Select	NP_001159.2:p.Ala134=
NM_001012270.2:c.284C>G	NP_001012270.1:p.Pro95Arg
NM_001012271.2:c.471C>G	NP_001012271.1:p.Ala157=