Canonical Allele Identifier: CA10641695
Gene: SMAD4 HGNC NCBI

Linked Data

dbSNP Id: rs56017493

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.51084041_51084044del , CM000680.2:g.51084041_51084044del GRCh38
NC_000018.9:g.48610411_48610414del , CM000680.1:g.48610411_48610414del GRCh37
NC_000018.8:g.46864409_46864412del NCBI36
NG_013013.2:g.121002_121005del , LRG_318:g.121002_121005del

Transcript Alleles

HGVS Amino-acid change
ENST00000588860.6:c.*5574_*5577del ENSP00000465878.2:n.*5574_*5577del
ENST00000589076.6:c.*5574_*5577del ENSP00000466934.2:n.*5574_*5577del
ENST00000589941.2:c.*5574_*5577del ENSP00000465874.2:n.*5574_*5577del
ENST00000590061.2:c.*5574_*5577del ENSP00000464772.2:n.*5574_*5577del
ENST00000688574.1:n.7341_7344del
ENST00000342988.8:c.*5574_*5577del MANE Select ENSP00000341551.3:n.*5574_*5577del
ENST00000342988.7:c.*5574_*5577del ENSP00000341551.3:n.*5574_*5577del
ENST00000398417.6:c.*5574_*5577del ENSP00000381452.1:n.*5574_*5577del
NM_005359.5:c.*5574_*5577del , LRG_318t1:c.*5574_*5577del NP_005350.1:n.*5574_*5577del
NM_005359.6:c.*5574_*5577del MANE Select NP_005350.1:n.*5574_*5577del