Canonical Allele Identifier: CA2735199876
Gene: SMAD4 HGNC NCBI

Linked Data

dbSNP Id: rs2144401281

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.51047194_51047195insG , CM000680.2:g.51047194_51047195insG GRCh38
NC_000018.9:g.48573564_48573565insG , CM000680.1:g.48573564_48573565insG GRCh37
NC_000018.8:g.46827562_46827563insG NCBI36
NG_013013.2:g.84155_84156insG , LRG_318:g.84155_84156insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000588860.6:c.148_149insG ENSP00000465878.2:p.Lys50ArgfsTer4
ENST00000589076.6:c.148_149insG ENSP00000466934.2:p.Lys50ArgfsTer4
ENST00000589941.2:c.148_149insG ENSP00000465874.2:p.Lys50ArgfsTer4
ENST00000590061.2:c.148_149insG ENSP00000464772.2:p.Lys50ArgfsTer4
ENST00000593223.2:c.148_149insG ENSP00000466118.2:p.Lys50ArgfsTer4
ENST00000611848.2:c.148_149insG ENSP00000478613.2:p.Lys50ArgfsTer4
ENST00000342988.8:c.148_149insG MANE Select ENSP00000341551.3:p.Lys50ArgfsTer4
ENST00000342988.7:c.148_149insG ENSP00000341551.3:p.Lys50ArgfsTer4
ENST00000398417.6:c.148_149insG ENSP00000381452.1:p.Lys50ArgfsTer4
ENST00000588745.5:c.148_149insG ENSP00000464901.1:p.Lys50ArgfsTer4
ENST00000588860.5:c.148_149insG ENSP00000465878.1:p.Lys50ArgfsTer4
ENST00000589076.5:c.148_149insG ENSP00000466934.1:p.Lys50ArgfsTer4
ENST00000589706.1:n.16_17insG
ENST00000589941.1:c.148_149insG ENSP00000465874.1:p.Lys50ArgfsTer4
ENST00000590061.1:c.148_149insG ENSP00000464772.1:p.Lys50ArgfsTer4
ENST00000590722.2:c.*171_*172insG ENSP00000465737.1:n.*171_*172insG
ENST00000591914.5:c.148_149insG ENSP00000466941.1:p.Lys50ArgfsTer4
ENST00000592186.5:c.148_149insG ENSP00000468611.1:p.Lys50ArgfsTer4
ENST00000592911.5:n.28-1492_28-1491insG
NM_005359.5:c.148_149insG , LRG_318t1:c.148_149insG NP_005350.1:p.Lys50ArgfsTer4
NM_005359.6:c.148_149insG MANE Select NP_005350.1:p.Lys50ArgfsTer4