Canonical Allele Identifier: CA2640134777

Gene: BIRC5

Linked Data

• gnomAD v4: 17-78224057-TTTTTTTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78224064_78224070del , CM000679.2:g.78224064_78224070del	GRCh38
NC_000017.10:g.76220145_76220151del , CM000679.1:g.76220145_76220151del	GRCh37
NC_000017.9:g.73731740_73731746del	NCBI36
NG_029069.1:g.14869_14875del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350051.8:c.*510_*516del MANE Select	ENSP00000324180.4:n.*510_*516del
ENST00000301633.8:c.*510_*516del	ENSP00000301633.3:n.*510_*516del
ENST00000350051.7:c.*510_*516del	ENSP00000324180.4:n.*510_*516del
ENST00000374948.6:c.*407_*413del	ENSP00000364086.1:n.*407_*413del
NM_001012270.1:c.*407_*413del	NP_001012270.1:n.*407_*413del
NM_001012271.1:c.*510_*516del	NP_001012271.1:n.*510_*516del
NM_001168.2:c.*510_*516del	NP_001159.2:n.*510_*516del
XR_243654.3:n.1141_1147del
XR_934452.1:n.1210_1216del
XR_243654.5:n.1141_1147del
XR_934452.3:n.1210_1216del
NM_001168.3:c.*510_*516del MANE Select	NP_001159.2:n.*510_*516del
NM_001012270.2:c.*407_*413del	NP_001012270.1:n.*407_*413del
NM_001012271.2:c.*510_*516del	NP_001012271.1:n.*510_*516del