Canonical Allele Identifier: CA2302987005

Gene: SMAD4

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51078506G= , CM000680.2:g.51078506G=	GRCh38
NC_000018.9:g.48604876G= , CM000680.1:g.48604876G=	GRCh37
NC_000018.8:g.46858874G=	NCBI36
NG_013013.2:g.115467G= , LRG_318:g.115467G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588860.6:c.*39G=	ENSP00000465878.2:n.*39G=
ENST00000589076.6:c.*39G=	ENSP00000466934.2:n.*39G=
ENST00000589941.2:c.*39G=	ENSP00000465874.2:n.*39G=
ENST00000590061.2:c.*39G=	ENSP00000464772.2:n.*39G=
ENST00000593223.2:c.*1695G=	ENSP00000466118.2:n.*1695G=
ENST00000611848.2:c.*350G=	ENSP00000478613.2:n.*350G=
ENST00000684953.1:n.3713G=
ENST00000685090.1:n.3628G=
ENST00000685232.1:n.1919G=
ENST00000688574.1:n.1806G=
ENST00000691124.1:n.4659G=
ENST00000342988.8:c.*39G= MANE Select	ENSP00000341551.3:n.*39G=
ENST00000342988.7:c.*39G=	ENSP00000341551.3:n.*39G=
ENST00000398417.6:c.*39G=	ENSP00000381452.1:n.*39G=
ENST00000586253.1:n.420G=
ENST00000591126.5:n.3699G=
ENST00000611848.1:c.1011G=
NM_005359.5:c.*39G= , LRG_318t1:c.*39G=	NP_005350.1:n.*39G=
NM_005359.6:c.*39G= MANE Select	NP_005350.1:n.*39G=