Canonical Allele Identifier: CA919900863
Gene: BIRC5 HGNC NCBI

Linked Data

dbSNP Id: rs17882139

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78223703_78223704insAAG , CM000679.2:g.78223703_78223704insAAG GRCh38
NC_000017.10:g.76219784_76219785insAAG , CM000679.1:g.76219784_76219785insAAG GRCh37
NC_000017.9:g.73731379_73731380insAAG NCBI36
NG_029069.1:g.14508_14509insAAG

Transcript Alleles

HGVS Amino-acid change
ENST00000350051.8:c.*149_*150insAAG MANE Select ENSP00000324180.4:n.*149_*150insAAG
ENST00000301633.8:c.*149_*150insAAG ENSP00000301633.3:n.*149_*150insAAG
ENST00000350051.7:c.*149_*150insAAG ENSP00000324180.4:n.*149_*150insAAG
ENST00000374948.6:c.*46_*47insAAG ENSP00000364086.1:n.*46_*47insAAG
ENST00000589892.1:n.594_595insAAG
NM_001012270.1:c.*46_*47insAAG NP_001012270.1:n.*46_*47insAAG
NM_001012271.1:c.*149_*150insAAG NP_001012271.1:n.*149_*150insAAG
NM_001168.2:c.*149_*150insAAG NP_001159.2:n.*149_*150insAAG
XR_243654.3:n.780_781insAAG
XR_934452.1:n.849_850insAAG
XR_243654.5:n.780_781insAAG
XR_934452.3:n.849_850insAAG
NM_001168.3:c.*149_*150insAAG MANE Select NP_001159.2:n.*149_*150insAAG
NM_001012270.2:c.*46_*47insAAG NP_001012270.1:n.*46_*47insAAG
NM_001012271.2:c.*149_*150insAAG NP_001012271.1:n.*149_*150insAAG