Canonical Allele Identifier: CA2641864671
Gene: SMAD4 HGNC NCBI

Linked Data

dbSNP Id: rs2144490823

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.51084338_51084342del , CM000680.2:g.51084338_51084342del GRCh38
NC_000018.9:g.48610708_48610712del , CM000680.1:g.48610708_48610712del GRCh37
NC_000018.8:g.46864706_46864710del NCBI36
NG_013013.2:g.121299_121303del , LRG_318:g.121299_121303del

Transcript Alleles

HGVS Amino-acid Change
ENST00000588860.6:c.*5871_*5875del ENSP00000465878.2:n.*5871_*5875del
ENST00000589076.6:c.*5871_*5875del ENSP00000466934.2:n.*5871_*5875del
ENST00000589941.2:c.*5871_*5875del ENSP00000465874.2:n.*5871_*5875del
ENST00000590061.2:c.*5871_*5875del ENSP00000464772.2:n.*5871_*5875del
ENST00000688574.1:n.7638_7642del
ENST00000342988.8:c.*5871_*5875del MANE Select ENSP00000341551.3:n.*5871_*5875del
ENST00000342988.7:c.*5871_*5875del ENSP00000341551.3:n.*5871_*5875del
ENST00000398417.6:c.*5871_*5875del ENSP00000381452.1:n.*5871_*5875del
NM_005359.5:c.*5871_*5875del , LRG_318t1:c.*5871_*5875del NP_005350.1:n.*5871_*5875del
NM_005359.6:c.*5871_*5875del MANE Select NP_005350.1:n.*5871_*5875del