Canonical Allele Identifier: CA2184419351

Gene: SMAD3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.67184823G= , CM000677.2:g.67184823G=	GRCh38
NC_000015.9:g.67477161G= , CM000677.1:g.67477161G=	GRCh37
NC_000015.8:g.65264215G=	NCBI36
NG_011990.1:g.123967G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558428.6:c.383G=	ENSP00000454165.2:p.Arg128=
ENST00000558739.2:c.653G=	ENSP00000453684.2:p.Arg218=
ENST00000558827.2:c.383G=	ENSP00000452767.2:p.Arg128=
ENST00000559460.6:c.653G=	ENSP00000453082.2:p.Arg218=
ENST00000560424.2:c.968G=	ENSP00000455540.2:p.Arg323=
ENST00000327367.9:c.968G= MANE Select	ENSP00000332973.4:p.Arg323=
ENST00000679624.1:c.653G=	ENSP00000505445.1:p.Arg218=
ENST00000680689.1:n.671G=
ENST00000681239.1:c.653G=	ENSP00000505641.1:p.Arg218=
ENST00000327367.8:c.968G=	ENSP00000332973.4:p.Arg323=
ENST00000439724.7:c.836G=	ENSP00000401133.3:p.Arg279=
ENST00000537194.6:c.383G=	ENSP00000445348.2:p.Arg128=
ENST00000540846.6:c.653G=	ENSP00000437757.2:p.Arg218=
ENST00000558894.5:c.557-2542G=	ENSP00000458060.1:n.557-2542G=
ENST00000560402.1:n.283-8050G=
ENST00000560424.1:c.49G=
NM_001145102.1:c.653G=	NP_001138574.1:p.Arg218=
NM_001145103.1:c.836G=	NP_001138575.1:p.Arg279=
NM_001145104.1:c.383G=	NP_001138576.1:p.Arg128=
NM_005902.3:c.968G=	NP_005893.1:p.Arg323=
XM_011521559.1:c.836G=	XP_011519861.1:p.Arg279=
XM_011521560.1:c.821G=	XP_011519862.1:p.Arg274=
XM_011521559.3:c.836G=	XP_011519861.1:p.Arg279=
NM_005902.4:c.968G= MANE Select	NP_005893.1:p.Arg323=
NM_001145102.2:c.653G=	NP_001138574.1:p.Arg218=
NM_001145103.2:c.836G=	NP_001138575.1:p.Arg279=
NM_001145104.2:c.383G=	NP_001138576.1:p.Arg128=