Canonical Allele Identifier: CA2302987003

Gene: SMAD4

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51078505G= , CM000680.2:g.51078505G=	GRCh38
NC_000018.9:g.48604875G= , CM000680.1:g.48604875G=	GRCh37
NC_000018.8:g.46858873G=	NCBI36
NG_013013.2:g.115466G= , LRG_318:g.115466G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588860.6:c.*38G=	ENSP00000465878.2:n.*38G=
ENST00000589076.6:c.*38G=	ENSP00000466934.2:n.*38G=
ENST00000589941.2:c.*38G=	ENSP00000465874.2:n.*38G=
ENST00000590061.2:c.*38G=	ENSP00000464772.2:n.*38G=
ENST00000593223.2:c.*1694G=	ENSP00000466118.2:n.*1694G=
ENST00000611848.2:c.*349G=	ENSP00000478613.2:n.*349G=
ENST00000684953.1:n.3712G=
ENST00000685090.1:n.3627G=
ENST00000685232.1:n.1918G=
ENST00000688574.1:n.1805G=
ENST00000691124.1:n.4658G=
ENST00000342988.8:c.*38G= MANE Select	ENSP00000341551.3:n.*38G=
ENST00000342988.7:c.*38G=	ENSP00000341551.3:n.*38G=
ENST00000398417.6:c.*38G=	ENSP00000381452.1:n.*38G=
ENST00000586253.1:n.419G=
ENST00000591126.5:n.3698G=
ENST00000611848.1:c.1010G=
NM_005359.5:c.*38G= , LRG_318t1:c.*38G=	NP_005350.1:n.*38G=
NM_005359.6:c.*38G= MANE Select	NP_005350.1:n.*38G=