Canonical Allele Identifier: CA2302971865

Gene: SMAD4

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51047286G= , CM000680.2:g.51047286G=	GRCh38
NC_000018.9:g.48573656G= , CM000680.1:g.48573656G=	GRCh37
NC_000018.8:g.46827654G=	NCBI36
NG_013013.2:g.84247G= , LRG_318:g.84247G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588860.6:c.240G=	ENSP00000465878.2:p.Gly80=
ENST00000589076.6:c.240G=	ENSP00000466934.2:p.Gly80=
ENST00000589941.2:c.240G=	ENSP00000465874.2:p.Gly80=
ENST00000590061.2:c.240G=	ENSP00000464772.2:p.Gly80=
ENST00000593223.2:c.240G=	ENSP00000466118.2:p.Gly80=
ENST00000611848.2:c.240G=	ENSP00000478613.2:p.Gly80=
ENST00000342988.8:c.240G= MANE Select	ENSP00000341551.3:p.Gly80=
ENST00000342988.7:c.240G=	ENSP00000341551.3:p.Gly80=
ENST00000398417.6:c.240G=	ENSP00000381452.1:p.Gly80=
ENST00000588745.5:c.240G=	ENSP00000464901.1:p.Gly80=
ENST00000588860.5:c.240G=	ENSP00000465878.1:p.Gly80=
ENST00000589076.5:c.240G=	ENSP00000466934.1:p.Gly80=
ENST00000589706.1:n.108G=
ENST00000589941.1:c.240G=	ENSP00000465874.1:p.Gly80=
ENST00000590061.1:c.240G=	ENSP00000464772.1:p.Gly80=
ENST00000590722.2:c.*263G=	ENSP00000465737.1:n.*263G=
ENST00000591914.5:c.240G=	ENSP00000466941.1:p.Gly80=
ENST00000592186.5:c.240G=	ENSP00000468611.1:p.Gly80=
ENST00000592911.5:n.28-1400G=
NM_005359.5:c.240G= , LRG_318t1:c.240G=	NP_005350.1:p.Gly80=
NM_005359.6:c.240G= MANE Select	NP_005350.1:p.Gly80=