Canonical Allele Identifier: CA2302986997

Gene: SMAD4

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51078493C= , CM000680.2:g.51078493C=	GRCh38
NC_000018.9:g.48604863C= , CM000680.1:g.48604863C=	GRCh37
NC_000018.8:g.46858861C=	NCBI36
NG_013013.2:g.115454C= , LRG_318:g.115454C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588860.6:c.*26C=	ENSP00000465878.2:n.*26C=
ENST00000589076.6:c.*26C=	ENSP00000466934.2:n.*26C=
ENST00000589941.2:c.*26C=	ENSP00000465874.2:n.*26C=
ENST00000590061.2:c.*26C=	ENSP00000464772.2:n.*26C=
ENST00000593223.2:c.*1682C=	ENSP00000466118.2:n.*1682C=
ENST00000611848.2:c.*337C=	ENSP00000478613.2:n.*337C=
ENST00000684953.1:n.3700C=
ENST00000685090.1:n.3615C=
ENST00000685232.1:n.1906C=
ENST00000688574.1:n.1793C=
ENST00000691124.1:n.4646C=
ENST00000342988.8:c.*26C= MANE Select	ENSP00000341551.3:n.*26C=
ENST00000342988.7:c.*26C=	ENSP00000341551.3:n.*26C=
ENST00000398417.6:c.*26C=	ENSP00000381452.1:n.*26C=
ENST00000586253.1:n.407C=
ENST00000591126.5:n.3686C=
ENST00000611848.1:c.998C=
NM_005359.5:c.*26C= , LRG_318t1:c.*26C=	NP_005350.1:n.*26C=
NM_005359.6:c.*26C= MANE Select	NP_005350.1:n.*26C=