Canonical Allele Identifier: CA2302977208

Gene: SMAD4

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51058355G= , CM000680.2:g.51058355G=	GRCh38
NC_000018.9:g.48584725G= , CM000680.1:g.48584725G=	GRCh37
NC_000018.8:g.46838723G=	NCBI36
NG_013013.2:g.95316G= , LRG_318:g.95316G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588860.6:c.803G=	ENSP00000465878.2:p.Trp268=
ENST00000589076.6:c.803G=	ENSP00000466934.2:p.Trp268=
ENST00000589941.2:c.803G=	ENSP00000465874.2:p.Trp268=
ENST00000590061.2:c.803G=	ENSP00000464772.2:p.Trp268=
ENST00000593223.2:c.803G=	ENSP00000466118.2:p.Trp268=
ENST00000611848.2:c.803G=	ENSP00000478613.2:p.Trp268=
ENST00000684953.1:n.2175G=
ENST00000685232.1:n.911G=
ENST00000688307.1:n.156-1511G=
ENST00000688574.1:n.911G=
ENST00000688903.1:n.1017G=
ENST00000690892.1:n.911G=
ENST00000342988.8:c.803G= MANE Select	ENSP00000341551.3:p.Trp268=
ENST00000342988.7:c.803G=	ENSP00000341551.3:p.Trp268=
ENST00000398417.6:c.803G=	ENSP00000381452.1:p.Trp268=
ENST00000588745.5:c.667+3362G=	ENSP00000464901.1:n.667+3362G=
ENST00000591126.5:n.2804G=
ENST00000592186.5:c.803G=	ENSP00000468611.1:p.Trp268=
ENST00000611848.1:c.3G=
NM_005359.5:c.803G= , LRG_318t1:c.803G=	NP_005350.1:p.Trp268=
NM_005359.6:c.803G= MANE Select	NP_005350.1:p.Trp268=