Canonical Allele Identifier: CA2630854347

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.681479_681481del , CM000678.2:g.681479_681481del GRCh38
NC_000016.9:g.731479_731481del , CM000678.1:g.731479_731481del GRCh37
NC_000016.8:g.671480_671482del NCBI36
NG_034141.1:g.6369_6371del

Transcript Alleles

HGVS Amino-acid Change
ENST00000219548.9:c.400_402del (STUB1) MANE Select ENSP00000219548.4:p.Asp134del
ENST00000219548.8:c.400_402del (STUB1) ENSP00000219548.4:p.Asp134del
ENST00000563505.5:n.496_498del (STUB1)
ENST00000564370.5:c.184_186del (STUB1) ENSP00000456875.1:p.Asp62del
ENST00000565677.5:c.184_186del (STUB1) ENSP00000457228.1:p.Asp62del
ENST00000566181.2:n.169_171del (STUB1)
ENST00000566408.5:c.117_119del (STUB1)
ENST00000567173.5:c.343_345del (STUB1) ENSP00000456591.1:p.Asp115del
ENST00000569248.5:n.974_976del (STUB1)
ENST00000620831.4:c.-50+38176_-50+38178del (MSLN) ENSP00000482893.1:n.-50+38176_-50+38178del
NM_001293197.1:c.184_186del (STUB1) NP_001280126.1:p.Asp62del
NM_005861.3:c.400_402del (STUB1) NP_005852.2:p.Asp134del
NM_005861.4:c.400_402del (STUB1) MANE Select NP_005852.2:p.Asp134del
NM_001293197.2:c.184_186del (STUB1) NP_001280126.1:p.Asp62del