Canonical Allele Identifier: CA2641864479
Gene: SMAD4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.51084006_51084029del , CM000680.2:g.51084006_51084029del GRCh38
NC_000018.9:g.48610376_48610399del , CM000680.1:g.48610376_48610399del GRCh37
NC_000018.8:g.46864374_46864397del NCBI36
NG_013013.2:g.120967_120990del , LRG_318:g.120967_120990del

Transcript Alleles

HGVS Amino-acid Change
ENST00000588860.6:c.*5539_*5562del ENSP00000465878.2:n.*5539_*5562del
ENST00000589076.6:c.*5539_*5562del ENSP00000466934.2:n.*5539_*5562del
ENST00000589941.2:c.*5539_*5562del ENSP00000465874.2:n.*5539_*5562del
ENST00000590061.2:c.*5539_*5562del ENSP00000464772.2:n.*5539_*5562del
ENST00000688574.1:n.7306_7329del
ENST00000342988.8:c.*5539_*5562del MANE Select ENSP00000341551.3:n.*5539_*5562del
ENST00000342988.7:c.*5539_*5562del ENSP00000341551.3:n.*5539_*5562del
ENST00000398417.6:c.*5539_*5562del ENSP00000381452.1:n.*5539_*5562del
NM_005359.5:c.*5539_*5562del , LRG_318t1:c.*5539_*5562del NP_005350.1:n.*5539_*5562del
NM_005359.6:c.*5539_*5562del MANE Select NP_005350.1:n.*5539_*5562del