Canonical Allele Identifier: CA2302986892

Gene: SMAD4

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51078324G= , CM000680.2:g.51078324G=	GRCh38
NC_000018.9:g.48604694G= , CM000680.1:g.48604694G=	GRCh37
NC_000018.8:g.46858692G=	NCBI36
NG_013013.2:g.115285G= , LRG_318:g.115285G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588860.6:c.1516G=	ENSP00000465878.2:p.Val506=
ENST00000589076.6:c.1516G=	ENSP00000466934.2:p.Val506=
ENST00000589941.2:c.1516G=	ENSP00000465874.2:p.Val506=
ENST00000590061.2:c.1516G=	ENSP00000464772.2:p.Val506=
ENST00000593223.2:c.*1513G=	ENSP00000466118.2:n.*1513G=
ENST00000611848.2:c.*168G=	ENSP00000478613.2:n.*168G=
ENST00000684953.1:n.3531G=
ENST00000685090.1:n.3446G=
ENST00000685232.1:n.1737G=
ENST00000688574.1:n.1624G=
ENST00000691124.1:n.4477G=
ENST00000342988.8:c.1516G= MANE Select	ENSP00000341551.3:p.Val506=
ENST00000342988.7:c.1516G=	ENSP00000341551.3:p.Val506=
ENST00000398417.6:c.1516G=	ENSP00000381452.1:p.Val506=
ENST00000586253.1:n.238G=
ENST00000588745.5:c.1228G=	ENSP00000464901.1:p.Val410=
ENST00000591126.5:n.3517G=
ENST00000592186.5:c.1163G=	ENSP00000468611.1:n.1163G=
ENST00000611848.1:c.829G=
NM_005359.5:c.1516G= , LRG_318t1:c.1516G=	NP_005350.1:p.Val506=
NM_005359.6:c.1516G= MANE Select	NP_005350.1:p.Val506=