Canonical Allele Identifier: CA294307138

Gene: BIRC5

Linked Data

• MyVariant Identifiers: chr17:g.76219783_76219784insAA (hg19) ; chr17:g.78223702_78223703insAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223702_78223703insAA , CM000679.2:g.78223702_78223703insAA	GRCh38
NC_000017.10:g.76219783_76219784insAA , CM000679.1:g.76219783_76219784insAA	GRCh37
NC_000017.9:g.73731378_73731379insAA	NCBI36
NG_029069.1:g.14507_14508insAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000350051.8:c.*148_*149insAA MANE Select	ENSP00000324180.4:n.*148_*149insAA
ENST00000301633.8:c.*148_*149insAA	ENSP00000301633.3:n.*148_*149insAA
ENST00000350051.7:c.*148_*149insAA	ENSP00000324180.4:n.*148_*149insAA
ENST00000374948.6:c.*45_*46insAA	ENSP00000364086.1:n.*45_*46insAA
ENST00000589892.1:n.593_594insAA
NM_001012270.1:c.*45_*46insAA	NP_001012270.1:n.*45_*46insAA
NM_001012271.1:c.*148_*149insAA	NP_001012271.1:n.*148_*149insAA
NM_001168.2:c.*148_*149insAA	NP_001159.2:n.*148_*149insAA
XR_243654.3:n.779_780insAA
XR_934452.1:n.848_849insAA
XR_243654.5:n.779_780insAA
XR_934452.3:n.848_849insAA
NM_001168.3:c.*148_*149insAA MANE Select	NP_001159.2:n.*148_*149insAA
NM_001012270.2:c.*45_*46insAA	NP_001012270.1:n.*45_*46insAA
NM_001012271.2:c.*148_*149insAA	NP_001012271.1:n.*148_*149insAA