Canonical Allele Identifier: CA2276860700
Gene: BIRC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78224039A= , CM000679.2:g.78224039A= GRCh38
NC_000017.10:g.76220120A= , CM000679.1:g.76220120A= GRCh37
NC_000017.9:g.73731715A= NCBI36
NG_029069.1:g.14844A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350051.8:c.*485A= MANE Select ENSP00000324180.4:n.*485A=
ENST00000301633.8:c.*485A= ENSP00000301633.3:n.*485A=
ENST00000350051.7:c.*485A= ENSP00000324180.4:n.*485A=
ENST00000374948.6:c.*382A= ENSP00000364086.1:n.*382A=
NM_001012270.1:c.*382A= NP_001012270.1:n.*382A=
NM_001012271.1:c.*485A= NP_001012271.1:n.*485A=
NM_001168.2:c.*485A= NP_001159.2:n.*485A=
XR_243654.3:n.1116A=
XR_934452.1:n.1185A=
XR_243654.5:n.1116A=
XR_934452.3:n.1185A=
NM_001168.3:c.*485A= MANE Select NP_001159.2:n.*485A=
NM_001012270.2:c.*382A= NP_001012270.1:n.*382A=
NM_001012271.2:c.*485A= NP_001012271.1:n.*485A=