Canonical Allele Identifier: CA2184414461

Gene: SMAD3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.67181256C= , CM000677.2:g.67181256C=	GRCh38
NC_000015.9:g.67473594C= , CM000677.1:g.67473594C=	GRCh37
NC_000015.8:g.65260648C=	NCBI36
NG_011990.1:g.120400C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558428.6:c.89C=	ENSP00000454165.2:p.Thr30=
ENST00000558739.2:c.359C=	ENSP00000453684.2:p.Thr120=
ENST00000558827.2:c.89C=	ENSP00000452767.2:p.Thr30=
ENST00000559460.6:c.359C=	ENSP00000453082.2:p.Thr120=
ENST00000560424.2:c.674C=	ENSP00000455540.2:p.Thr225=
ENST00000327367.9:c.674C= MANE Select	ENSP00000332973.4:p.Thr225=
ENST00000679624.1:c.359C=	ENSP00000505445.1:p.Thr120=
ENST00000680689.1:n.377C=
ENST00000681239.1:c.359C=	ENSP00000505641.1:p.Thr120=
ENST00000327367.8:c.674C=	ENSP00000332973.4:p.Thr225=
ENST00000439724.7:c.542C=	ENSP00000401133.3:p.Thr181=
ENST00000537194.6:c.89C=	ENSP00000445348.2:p.Thr30=
ENST00000540846.6:c.359C=	ENSP00000437757.2:p.Thr120=
ENST00000558428.5:c.89C=	ENSP00000454165.1:p.Thr30=
ENST00000558827.1:c.89C=	ENSP00000452767.1:p.Thr30=
ENST00000558894.5:c.359C=	ENSP00000458060.1:p.Thr120=
ENST00000560402.1:n.282+6672C=
NM_001145102.1:c.359C=	NP_001138574.1:p.Thr120=
NM_001145103.1:c.542C=	NP_001138575.1:p.Thr181=
NM_001145104.1:c.89C=	NP_001138576.1:p.Thr30=
NM_005902.3:c.674C=	NP_005893.1:p.Thr225=
XM_011521559.1:c.542C=	XP_011519861.1:p.Thr181=
XM_011521560.1:c.527C=	XP_011519862.1:p.Thr176=
XM_011521559.3:c.542C=	XP_011519861.1:p.Thr181=
NM_005902.4:c.674C= MANE Select	NP_005893.1:p.Thr225=
NM_001145102.2:c.359C=	NP_001138574.1:p.Thr120=
NM_001145103.2:c.542C=	NP_001138575.1:p.Thr181=
NM_001145104.2:c.89C=	NP_001138576.1:p.Thr30=