Canonical Allele Identifier: CA2640134792
Gene: BIRC5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78224074_78224077dup , CM000679.2:g.78224074_78224077dup GRCh38
NC_000017.10:g.76220155_76220158dup , CM000679.1:g.76220155_76220158dup GRCh37
NC_000017.9:g.73731750_73731753dup NCBI36
NG_029069.1:g.14879_14882dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000350051.8:c.*520_*523dup MANE Select ENSP00000324180.4:n.*520_*523dup
ENST00000301633.8:c.*520_*523dup ENSP00000301633.3:n.*520_*523dup
ENST00000350051.7:c.*520_*523dup ENSP00000324180.4:n.*520_*523dup
ENST00000374948.6:c.*417_*420dup ENSP00000364086.1:n.*417_*420dup
NM_001012270.1:c.*417_*420dup NP_001012270.1:n.*417_*420dup
NM_001012271.1:c.*520_*523dup NP_001012271.1:n.*520_*523dup
NM_001168.2:c.*520_*523dup NP_001159.2:n.*520_*523dup
XR_243654.3:n.1151_1154dup
XR_934452.1:n.1220_1223dup
XR_243654.5:n.1151_1154dup
XR_934452.3:n.1220_1223dup
NM_001168.3:c.*520_*523dup MANE Select NP_001159.2:n.*520_*523dup
NM_001012270.2:c.*417_*420dup NP_001012270.1:n.*417_*420dup
NM_001012271.2:c.*520_*523dup NP_001012271.1:n.*520_*523dup