Canonical Allele Identifier: CA2302980591

Gene: SMAD4

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51065548C= , CM000680.2:g.51065548C=	GRCh38
NC_000018.9:g.48591918C= , CM000680.1:g.48591918C=	GRCh37
NC_000018.8:g.46845916C=	NCBI36
NG_013013.2:g.102509C= , LRG_318:g.102509C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588860.6:c.1081C=	ENSP00000465878.2:p.Arg361=
ENST00000589076.6:c.1081C=	ENSP00000466934.2:p.Arg361=
ENST00000589941.2:c.1081C=	ENSP00000465874.2:p.Arg361=
ENST00000590061.2:c.1081C=	ENSP00000464772.2:p.Arg361=
ENST00000593223.2:c.1081C=	ENSP00000466118.2:p.Arg361=
ENST00000611848.2:c.1081C=	ENSP00000478613.2:p.Arg361=
ENST00000684953.1:n.2453C=
ENST00000685090.1:n.1532C=
ENST00000685232.1:n.1189C=
ENST00000688307.1:n.332C=
ENST00000688574.1:n.1189C=
ENST00000688903.1:n.1295C=
ENST00000691124.1:n.2563C=
ENST00000342988.8:c.1081C= MANE Select	ENSP00000341551.3:p.Arg361=
ENST00000342988.7:c.1081C=	ENSP00000341551.3:p.Arg361=
ENST00000398417.6:c.1081C=	ENSP00000381452.1:p.Arg361=
ENST00000588745.5:c.793C=	ENSP00000464901.1:p.Arg265=
ENST00000591126.5:n.3082C=
ENST00000592186.5:c.955+5632C=	ENSP00000468611.1:n.955+5632C=
ENST00000611848.1:c.281C=
NM_005359.5:c.1081C= , LRG_318t1:c.1081C=	NP_005350.1:p.Arg361=
NM_005359.6:c.1081C= MANE Select	NP_005350.1:p.Arg361=