Canonical Allele Identifier: CA401215690

Gene: BIRC5

Linked Data

• MyVariant Identifiers: chr17:g.76219703A>C (hg19) ; chr17:g.78223622A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223622A>C , CM000679.2:g.78223622A>C	GRCh38
NC_000017.10:g.76219703A>C , CM000679.1:g.76219703A>C	GRCh37
NC_000017.9:g.73731298A>C	NCBI36
NG_029069.1:g.14427A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*68A>C MANE Select	ENSP00000324180.4:n.*68A>C
ENST00000301633.8:c.*68A>C	ENSP00000301633.3:n.*68A>C
ENST00000350051.7:c.*68A>C	ENSP00000324180.4:n.*68A>C
ENST00000374948.6:c.379A>C	ENSP00000364086.1:p.Thr127Pro
ENST00000589892.1:n.513A>C
NM_001012270.1:c.379A>C	NP_001012270.1:p.Thr127Pro
NM_001012271.1:c.*68A>C	NP_001012271.1:n.*68A>C
NM_001168.2:c.*68A>C	NP_001159.2:n.*68A>C
XR_243654.3:n.699A>C
XR_934452.1:n.768A>C
XR_243654.5:n.699A>C
XR_934452.3:n.768A>C
NM_001168.3:c.*68A>C MANE Select	NP_001159.2:n.*68A>C
NM_001012270.2:c.379A>C	NP_001012270.1:p.Thr127Pro
NM_001012271.2:c.*68A>C	NP_001012271.1:n.*68A>C