Canonical Allele Identifier: CA2184411667

Gene: SMAD3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.67166191C= , CM000677.2:g.67166191C=	GRCh38
NC_000015.9:g.67458529C= , CM000677.1:g.67458529C=	GRCh37
NC_000015.8:g.65245583C=	NCBI36
NG_011990.1:g.105335C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558739.2:c.218-588C=	ENSP00000453684.2:n.218-588C=
ENST00000559460.6:c.218-588C=	ENSP00000453082.2:n.218-588C=
ENST00000560424.2:c.533-588C=	ENSP00000455540.2:n.533-588C=
ENST00000327367.9:c.533-588C= MANE Select	ENSP00000332973.4:n.533-588C=
ENST00000679624.1:c.218-588C=	ENSP00000505445.1:n.218-588C=
ENST00000681239.1:c.218-588C=	ENSP00000505641.1:n.218-588C=
ENST00000327367.8:c.533-588C=	ENSP00000332973.4:n.533-588C=
ENST00000439724.7:c.401-588C=	ENSP00000401133.3:n.401-588C=
ENST00000537194.6:c.-56C=	ENSP00000445348.2:n.-56C=
ENST00000540846.6:c.218-588C=	ENSP00000437757.2:n.218-588C=
ENST00000558894.5:c.218-588C=	ENSP00000458060.1:n.218-588C=
ENST00000559460.5:c.218-588C=	ENSP00000453082.1:n.218-588C=
ENST00000559937.1:n.383-588C=
ENST00000560175.5:c.218-588C=	ENSP00000455095.1:n.218-588C=
NM_001145102.1:c.218-588C=	NP_001138574.1:n.218-588C=
NM_001145103.1:c.401-588C=	NP_001138575.1:n.401-588C=
NM_001145104.1:c.-56C=	NP_001138576.1:n.-56C=
NM_005902.3:c.533-588C=	NP_005893.1:n.533-588C=
XM_011521559.1:c.401-588C=	XP_011519861.1:n.401-588C=
XM_011521560.1:c.386-588C=	XP_011519862.1:n.386-588C=
XM_011521559.3:c.401-588C=	XP_011519861.1:n.401-588C=
NM_005902.4:c.533-588C= MANE Select	NP_005893.1:n.533-588C=
NM_001145102.2:c.218-588C=	NP_001138574.1:n.218-588C=
NM_001145103.2:c.401-588C=	NP_001138575.1:n.401-588C=
NM_001145104.2:c.-56C=	NP_001138576.1:n.-56C=