Canonical Allele Identifier: CA401215483

Gene: BIRC5

Linked Data

• MyVariant Identifiers: chr17:g.76219677A>C (hg19) ; chr17:g.78223596A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223596A>C , CM000679.2:g.78223596A>C	GRCh38
NC_000017.10:g.76219677A>C , CM000679.1:g.76219677A>C	GRCh37
NC_000017.9:g.73731272A>C	NCBI36
NG_029069.1:g.14401A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*42A>C MANE Select	ENSP00000324180.4:n.*42A>C
ENST00000301633.8:c.*42A>C	ENSP00000301633.3:n.*42A>C
ENST00000350051.7:c.*42A>C	ENSP00000324180.4:n.*42A>C
ENST00000374948.6:c.353A>C	ENSP00000364086.1:p.His118Pro
ENST00000589892.1:n.487A>C
NM_001012270.1:c.353A>C	NP_001012270.1:p.His118Pro
NM_001012271.1:c.*42A>C	NP_001012271.1:n.*42A>C
NM_001168.2:c.*42A>C	NP_001159.2:n.*42A>C
XR_243654.3:n.673A>C
XR_934452.1:n.742A>C
XR_243654.5:n.673A>C
XR_934452.3:n.742A>C
NM_001168.3:c.*42A>C MANE Select	NP_001159.2:n.*42A>C
NM_001012270.2:c.353A>C	NP_001012270.1:p.His118Pro
NM_001012271.2:c.*42A>C	NP_001012271.1:n.*42A>C