Canonical Allele Identifier: CA2805525114

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.681361_681362insGGAG , CM000678.2:g.681361_681362insGGAG GRCh38
NC_000016.9:g.731361_731362insGGAG , CM000678.1:g.731361_731362insGGAG GRCh37
NC_000016.8:g.671362_671363insGGAG NCBI36
NG_034141.1:g.6251_6252insGGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000219548.9:c.358+11_358+12insGGAG (STUB1) MANE Select ENSP00000219548.4:n.358+11_358+12insGGAG
ENST00000219548.8:c.358+11_358+12insGGAG (STUB1) ENSP00000219548.4:n.358+11_358+12insGGAG
ENST00000563505.5:n.454+11_454+12insGGAG (STUB1)
ENST00000564370.5:c.142+11_142+12insGGAG (STUB1) ENSP00000456875.1:n.142+11_142+12insGGAG
ENST00000565677.5:c.142+11_142+12insGGAG (STUB1) ENSP00000457228.1:n.142+11_142+12insGGAG
ENST00000566181.2:n.127+11_127+12insGGAG (STUB1)
ENST00000566408.5:c.75+11_75+12insGGAG (STUB1)
ENST00000567173.5:c.301+11_301+12insGGAG (STUB1) ENSP00000456591.1:n.301+11_301+12insGGAG
ENST00000567790.1:n.399_400insGGAG (STUB1)
ENST00000569248.5:n.932+11_932+12insGGAG (STUB1)
ENST00000620831.4:c.-50+38058_-50+38059insGGAG (MSLN) ENSP00000482893.1:n.-50+38058_-50+38059insGGAG
NM_001293197.1:c.142+11_142+12insGGAG (STUB1) NP_001280126.1:n.142+11_142+12insGGAG
NM_005861.3:c.358+11_358+12insGGAG (STUB1) NP_005852.2:n.358+11_358+12insGGAG
NM_005861.4:c.358+11_358+12insGGAG (STUB1) MANE Select NP_005852.2:n.358+11_358+12insGGAG
NM_001293197.2:c.142+11_142+12insGGAG (STUB1) NP_001280126.1:n.142+11_142+12insGGAG