Canonical Allele Identifier: CA502082028

Gene: BIRC5

Linked Data

• dbSNP Id: rs377394472
• MyVariant Identifiers: chr17:g.76219687T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223606T>G , CM000679.2:g.78223606T>G	GRCh38
NC_000017.10:g.76219687T>G , CM000679.1:g.76219687T>G	GRCh37
NC_000017.9:g.73731282T>G	NCBI36
NG_029069.1:g.14411T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*52T>G MANE Select	ENSP00000324180.4:n.*52T>G
ENST00000301633.8:c.*52T>G	ENSP00000301633.3:n.*52T>G
ENST00000350051.7:c.*52T>G	ENSP00000324180.4:n.*52T>G
ENST00000374948.6:c.363T>G	ENSP00000364086.1:p.Gly121=
ENST00000589892.1:n.497T>G
NM_001012270.1:c.363T>G	NP_001012270.1:p.Gly121=
NM_001012271.1:c.*52T>G	NP_001012271.1:n.*52T>G
NM_001168.2:c.*52T>G	NP_001159.2:n.*52T>G
XR_243654.3:n.683T>G
XR_934452.1:n.752T>G
XR_243654.5:n.683T>G
XR_934452.3:n.752T>G
NM_001168.3:c.*52T>G MANE Select	NP_001159.2:n.*52T>G
NM_001012270.2:c.363T>G	NP_001012270.1:p.Gly121=
NM_001012271.2:c.*52T>G	NP_001012271.1:n.*52T>G