Canonical Allele Identifier: CA986568316
Gene: BIRC5 HGNC NCBI

Linked Data

dbSNP Id: rs2076533244

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78224051del , CM000679.2:g.78224051del GRCh38
NC_000017.10:g.76220132del , CM000679.1:g.76220132del GRCh37
NC_000017.9:g.73731727del NCBI36
NG_029069.1:g.14856del

Transcript Alleles

HGVS Amino-acid Change
ENST00000350051.8:c.*497del MANE Select ENSP00000324180.4:n.*497del
ENST00000301633.8:c.*497del ENSP00000301633.3:n.*497del
ENST00000350051.7:c.*497del ENSP00000324180.4:n.*497del
ENST00000374948.6:c.*394del ENSP00000364086.1:n.*394del
NM_001012270.1:c.*394del NP_001012270.1:n.*394del
NM_001012271.1:c.*497del NP_001012271.1:n.*497del
NM_001168.2:c.*497del NP_001159.2:n.*497del
XR_243654.3:n.1128del
XR_934452.1:n.1197del
XR_243654.5:n.1128del
XR_934452.3:n.1197del
NM_001168.3:c.*497del MANE Select NP_001159.2:n.*497del
NM_001012270.2:c.*394del NP_001012270.1:n.*394del
NM_001012271.2:c.*497del NP_001012271.1:n.*497del