Canonical Allele Identifier: CA2302981538
Gene: SMAD4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.51067124_51067126delinsCAG , CM000680.2:g.51067124_51067126delinsCAG GRCh38
NC_000018.9:g.48593494_48593496delinsCAG , CM000680.1:g.48593494_48593496delinsCAG GRCh37
NC_000018.8:g.46847492_46847494delinsCAG NCBI36
NG_013013.2:g.104085_104087delinsCAG , LRG_318:g.104085_104087delinsCAG

Transcript Alleles

HGVS Amino-acid change
ENST00000588860.6:c.1245_1247delinsCAG ENSP00000465878.2:p.Asp415=
ENST00000589076.6:c.1245_1247delinsCAG ENSP00000466934.2:p.Asp415=
ENST00000589941.2:c.1245_1247delinsCAG ENSP00000465874.2:p.Asp415=
ENST00000590061.2:c.1245_1247delinsCAG ENSP00000464772.2:p.Asp415=
ENST00000593223.2:c.1245_1247delinsCAG ENSP00000466118.2:p.Asp415=
ENST00000611848.2:c.1245_1247delinsCAG ENSP00000478613.2:p.Asp415=
ENST00000684953.1:n.2617_2619delinsCAG
ENST00000685090.1:n.1696_1698delinsCAG
ENST00000685232.1:n.1353_1355delinsCAG
ENST00000688574.1:n.1353_1355delinsCAG
ENST00000691124.1:n.2727_2729delinsCAG
ENST00000342988.8:c.1245_1247delinsCAG MANE Select ENSP00000341551.3:p.Asp415=
ENST00000342988.7:c.1245_1247delinsCAG ENSP00000341551.3:p.Asp415=
ENST00000398417.6:c.1245_1247delinsCAG ENSP00000381452.1:p.Asp415=
ENST00000588745.5:c.957_959delinsCAG ENSP00000464901.1:p.Asp319=
ENST00000590499.1:n.303_305delinsCAG
ENST00000591126.5:n.3246_3248delinsCAG
ENST00000592186.5:c.955+7208_955+7210delinsCAG ENSP00000468611.1:n.955+7208_955+7210deli...
ENST00000593223.1:c.12_14delinsCAG ENSP00000466118.1:p.Asp4=
ENST00000611848.1:c.445_447delinsCAG
NM_005359.5:c.1245_1247delinsCAG , LRG_318t1:c.1245_1247delinsCAG NP_005350.1:p.Asp415=
NM_005359.6:c.1245_1247delinsCAG MANE Select NP_005350.1:p.Asp415=