Canonical Allele Identifier: CA8798669

Gene: BIRC5

Linked Data

• dbSNP Id: rs17882139
• ExAC: 17:76219784 T / TAA
• gnomAD v2: 17-76219784-T-TAA
• gnomAD v3: 17-78223703-T-TAA
• gnomAD v4: 17-78223703-T-TAA
• COSMIC: COSM5713323
• MyVariant Identifiers: chr17:g.76219784_76219785insAA (hg19) ; chr17:g.78223703_78223704insAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223703_78223704insAA , CM000679.2:g.78223703_78223704insAA	GRCh38
NC_000017.10:g.76219784_76219785insAA , CM000679.1:g.76219784_76219785insAA	GRCh37
NC_000017.9:g.73731379_73731380insAA	NCBI36
NG_029069.1:g.14508_14509insAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000350051.8:c.*149_*150insAA MANE Select	ENSP00000324180.4:n.*149_*150insAA
ENST00000301633.8:c.*149_*150insAA	ENSP00000301633.3:n.*149_*150insAA
ENST00000350051.7:c.*149_*150insAA	ENSP00000324180.4:n.*149_*150insAA
ENST00000374948.6:c.*46_*47insAA	ENSP00000364086.1:n.*46_*47insAA
ENST00000589892.1:n.594_595insAA
NM_001012270.1:c.*46_*47insAA	NP_001012270.1:n.*46_*47insAA
NM_001012271.1:c.*149_*150insAA	NP_001012271.1:n.*149_*150insAA
NM_001168.2:c.*149_*150insAA	NP_001159.2:n.*149_*150insAA
XR_243654.3:n.780_781insAA
XR_934452.1:n.849_850insAA
XR_243654.5:n.780_781insAA
XR_934452.3:n.849_850insAA
NM_001168.3:c.*149_*150insAA MANE Select	NP_001159.2:n.*149_*150insAA
NM_001012270.2:c.*46_*47insAA	NP_001012270.1:n.*46_*47insAA
NM_001012271.2:c.*149_*150insAA	NP_001012271.1:n.*149_*150insAA