Canonical Allele Identifier: CA2640136332
Gene: BIRC5 HGNC NCBI

Linked Data

gnomAD v4: 17-78225373-TACATGTCC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.78225383_78225390del , CM000679.2:g.78225383_78225390del GRCh38
NC_000017.10:g.76221464_76221471del , CM000679.1:g.76221464_76221471del GRCh37
NC_000017.9:g.73733059_73733066del NCBI36
NG_029069.1:g.16188_16195del

Transcript Alleles

HGVS Amino-acid change
ENST00000350051.8:c.*1829_*1836del MANE Select ENSP00000324180.4:n.*1829_*1836del
ENST00000301633.8:c.*1829_*1836del ENSP00000301633.3:n.*1829_*1836del
ENST00000350051.7:c.*1829_*1836del ENSP00000324180.4:n.*1829_*1836del
ENST00000374948.6:c.*1726_*1733del ENSP00000364086.1:n.*1726_*1733del
NM_001012270.1:c.*1726_*1733del NP_001012270.1:n.*1726_*1733del
NM_001012271.1:c.*1829_*1836del NP_001012271.1:n.*1829_*1836del
NM_001168.2:c.*1829_*1836del NP_001159.2:n.*1829_*1836del
NM_001168.3:c.*1829_*1836del MANE Select NP_001159.2:n.*1829_*1836del
NM_001012270.2:c.*1726_*1733del NP_001012270.1:n.*1726_*1733del
NM_001012271.2:c.*1829_*1836del NP_001012271.1:n.*1829_*1836del
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