Canonical Allele Identifier: CA2641864517
Gene: SMAD4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.51084035_51084036insGCAC , CM000680.2:g.51084035_51084036insGCAC GRCh38
NC_000018.9:g.48610405_48610406insGCAC , CM000680.1:g.48610405_48610406insGCAC GRCh37
NC_000018.8:g.46864403_46864404insGCAC NCBI36
NG_013013.2:g.120996_120997insGCAC , LRG_318:g.120996_120997insGCAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000588860.6:c.*5568_*5569insGCAC ENSP00000465878.2:n.*5568_*5569insGCAC
ENST00000589076.6:c.*5568_*5569insGCAC ENSP00000466934.2:n.*5568_*5569insGCAC
ENST00000589941.2:c.*5568_*5569insGCAC ENSP00000465874.2:n.*5568_*5569insGCAC
ENST00000590061.2:c.*5568_*5569insGCAC ENSP00000464772.2:n.*5568_*5569insGCAC
ENST00000688574.1:n.7335_7336insGCAC
ENST00000342988.8:c.*5568_*5569insGCAC MANE Select ENSP00000341551.3:n.*5568_*5569insGCAC
ENST00000342988.7:c.*5568_*5569insGCAC ENSP00000341551.3:n.*5568_*5569insGCAC
ENST00000398417.6:c.*5568_*5569insGCAC ENSP00000381452.1:n.*5568_*5569insGCAC
NM_005359.5:c.*5568_*5569insGCAC , LRG_318t1:c.*5568_*5569insGCAC NP_005350.1:n.*5568_*5569insGCAC
NM_005359.6:c.*5568_*5569insGCAC MANE Select NP_005350.1:n.*5568_*5569insGCAC