Canonical Allele Identifier: CA502082679

Gene: BIRC5

Linked Data

• MyVariant Identifiers: chr17:g.76219761A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223680A>T , CM000679.2:g.78223680A>T	GRCh38
NC_000017.10:g.76219761A>T , CM000679.1:g.76219761A>T	GRCh37
NC_000017.9:g.73731356A>T	NCBI36
NG_029069.1:g.14485A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*126A>T MANE Select	ENSP00000324180.4:n.*126A>T
ENST00000301633.8:c.*126A>T	ENSP00000301633.3:n.*126A>T
ENST00000350051.7:c.*126A>T	ENSP00000324180.4:n.*126A>T
ENST00000374948.6:c.*23A>T	ENSP00000364086.1:n.*23A>T
ENST00000589892.1:n.571A>T
NM_001012270.1:c.*23A>T	NP_001012270.1:n.*23A>T
NM_001012271.1:c.*126A>T	NP_001012271.1:n.*126A>T
NM_001168.2:c.*126A>T	NP_001159.2:n.*126A>T
XR_243654.3:n.757A>T
XR_934452.1:n.826A>T
XR_243654.5:n.757A>T
XR_934452.3:n.826A>T
NM_001168.3:c.*126A>T MANE Select	NP_001159.2:n.*126A>T
NM_001012270.2:c.*23A>T	NP_001012270.1:n.*23A>T
NM_001012271.2:c.*126A>T	NP_001012271.1:n.*126A>T