Canonical Allele Identifier: CA2302978001

Gene: SMAD4

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51059913C= , CM000680.2:g.51059913C=	GRCh38
NC_000018.9:g.48586283C= , CM000680.1:g.48586283C=	GRCh37
NC_000018.8:g.46840281C=	NCBI36
NG_013013.2:g.96874C= , LRG_318:g.96874C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588860.6:c.952C=	ENSP00000465878.2:p.Pro318=
ENST00000589076.6:c.952C=	ENSP00000466934.2:p.Pro318=
ENST00000589941.2:c.952C=	ENSP00000465874.2:p.Pro318=
ENST00000590061.2:c.952C=	ENSP00000464772.2:p.Pro318=
ENST00000593223.2:c.952C=	ENSP00000466118.2:p.Pro318=
ENST00000611848.2:c.952C=	ENSP00000478613.2:p.Pro318=
ENST00000684953.1:n.2324C=
ENST00000685090.1:n.1403C=
ENST00000685232.1:n.1060C=
ENST00000688307.1:n.203C=
ENST00000688574.1:n.1060C=
ENST00000688903.1:n.1166C=
ENST00000690892.1:n.1060C=
ENST00000342988.8:c.952C= MANE Select	ENSP00000341551.3:p.Pro318=
ENST00000342988.7:c.952C=	ENSP00000341551.3:p.Pro318=
ENST00000398417.6:c.952C=	ENSP00000381452.1:p.Pro318=
ENST00000588745.5:c.667+4920C=	ENSP00000464901.1:n.667+4920C=
ENST00000591126.5:n.2953C=
ENST00000592186.5:c.952C=	ENSP00000468611.1:p.Pro318=
ENST00000611848.1:c.152C=
NM_005359.5:c.952C= , LRG_318t1:c.952C=	NP_005350.1:p.Pro318=
NM_005359.6:c.952C= MANE Select	NP_005350.1:p.Pro318=