Canonical Allele Identifier: CA2276860457

Gene: BIRC5

Linked Data

• dbSNP Id: rs2076527725
• gnomAD v4: 17-78223349-GTTTA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78223354_78223357del , CM000679.2:g.78223354_78223357del	GRCh38
NC_000017.10:g.76219435_76219438del , CM000679.1:g.76219435_76219438del	GRCh37
NC_000017.9:g.73731030_73731033del	NCBI36
NG_029069.1:g.14159_14162del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.340-111_340-108del MANE Select	ENSP00000324180.4:n.340-111_340-108del
ENST00000301633.8:c.409-111_409-108del	ENSP00000301633.3:n.409-111_409-108del
ENST00000350051.7:c.340-111_340-108del	ENSP00000324180.4:n.340-111_340-108del
ENST00000374948.6:c.222-111_222-108del	ENSP00000364086.1:n.222-111_222-108del
ENST00000589892.1:n.356-111_356-108del
ENST00000590925.6:c.*142-111_*142-108del	ENSP00000467336.1:n.*142-111_*142-108del
NM_001012270.1:c.222-111_222-108del	NP_001012270.1:n.222-111_222-108del
NM_001012271.1:c.409-111_409-108del	NP_001012271.1:n.409-111_409-108del
NM_001168.2:c.340-111_340-108del	NP_001159.2:n.340-111_340-108del
XR_243654.3:n.542-111_542-108del
XR_934452.1:n.611-111_611-108del
XR_243654.5:n.542-111_542-108del
XR_934452.3:n.611-111_611-108del
NM_001168.3:c.340-111_340-108del MANE Select	NP_001159.2:n.340-111_340-108del
NM_001012270.2:c.222-111_222-108del	NP_001012270.1:n.222-111_222-108del
NM_001012271.2:c.409-111_409-108del	NP_001012271.1:n.409-111_409-108del