Canonical Allele Identifier: CA2302986883

Gene: SMAD4

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51078308A= , CM000680.2:g.51078308A=	GRCh38
NC_000018.9:g.48604678A= , CM000680.1:g.48604678A=	GRCh37
NC_000018.8:g.46858676A=	NCBI36
NG_013013.2:g.115269A= , LRG_318:g.115269A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588860.6:c.1500A=	ENSP00000465878.2:p.Ile500=
ENST00000589076.6:c.1500A=	ENSP00000466934.2:p.Ile500=
ENST00000589941.2:c.1500A=	ENSP00000465874.2:p.Ile500=
ENST00000590061.2:c.1500A=	ENSP00000464772.2:p.Ile500=
ENST00000593223.2:c.*1497A=	ENSP00000466118.2:n.*1497A=
ENST00000611848.2:c.*152A=	ENSP00000478613.2:n.*152A=
ENST00000684953.1:n.3515A=
ENST00000685090.1:n.3430A=
ENST00000685232.1:n.1721A=
ENST00000688574.1:n.1608A=
ENST00000691124.1:n.4461A=
ENST00000342988.8:c.1500A= MANE Select	ENSP00000341551.3:p.Ile500=
ENST00000342988.7:c.1500A=	ENSP00000341551.3:p.Ile500=
ENST00000398417.6:c.1500A=	ENSP00000381452.1:p.Ile500=
ENST00000586253.1:n.222A=
ENST00000588745.5:c.1212A=	ENSP00000464901.1:p.Ile404=
ENST00000591126.5:n.3501A=
ENST00000592186.5:c.1147A=	ENSP00000468611.1:n.1147A=
ENST00000611848.1:c.813A=
NM_005359.5:c.1500A= , LRG_318t1:c.1500A=	NP_005350.1:p.Ile500=
NM_005359.6:c.1500A= MANE Select	NP_005350.1:p.Ile500=