Canonical Allele Identifier: CA990240776
Gene: SMAD4 HGNC NCBI

Linked Data

dbSNP Id: rs1909553758

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.51046729_51046731del , CM000680.2:g.51046729_51046731del GRCh38
NC_000018.9:g.48573099_48573101del , CM000680.1:g.48573099_48573101del GRCh37
NC_000018.8:g.46827097_46827099del NCBI36
NG_013013.2:g.83690_83692del , LRG_318:g.83690_83692del

Transcript Alleles

HGVS Amino-acid Change
ENST00000588860.6:c.-127-191_-127-189del ENSP00000465878.2:n.-127-191_-127-189del
ENST00000589076.6:c.-127-191_-127-189del ENSP00000466934.2:n.-127-191_-127-189del
ENST00000589941.2:c.-127-191_-127-189del ENSP00000465874.2:n.-127-191_-127-189del
ENST00000590061.2:c.-59-259_-59-257del ENSP00000464772.2:n.-59-259_-59-257del
ENST00000593223.2:c.-127-191_-127-189del ENSP00000466118.2:n.-127-191_-127-189del
ENST00000342988.8:c.-127-191_-127-189del MANE Select ENSP00000341551.3:n.-127-191_-127-189del
ENST00000342988.7:c.-127-191_-127-189del ENSP00000341551.3:n.-127-191_-127-189del
ENST00000398417.6:c.-127-191_-127-189del ENSP00000381452.1:n.-127-191_-127-189del
ENST00000588256.1:n.335-191_335-189del
ENST00000588860.5:c.-127-191_-127-189del ENSP00000465878.1:n.-127-191_-127-189del
ENST00000589076.5:c.-127-191_-127-189del ENSP00000466934.1:n.-127-191_-127-189del
ENST00000589941.1:c.-127-191_-127-189del ENSP00000465874.1:n.-127-191_-127-189del
ENST00000590061.1:c.-59-259_-59-257del ENSP00000464772.1:n.-59-259_-59-257del
ENST00000590722.2:c.158-191_158-189del ENSP00000465737.1:n.158-191_158-189del
ENST00000591914.5:c.-127-191_-127-189del ENSP00000466941.1:n.-127-191_-127-189del
ENST00000592911.5:n.28-1957_28-1955del
NM_005359.5:c.-127-191_-127-189del , LRG_318t1:c.-127-191_-127-189del NP_005350.1:n.-127-191_-127-189del
NM_005359.6:c.-127-191_-127-189del MANE Select NP_005350.1:n.-127-191_-127-189del