Canonical Allele Identifier: CA490917726

Gene: SMAD3

Linked Data

• MyVariant Identifiers: chr15:g.67479789T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.67187451T>C , CM000677.2:g.67187451T>C	GRCh38
NC_000015.9:g.67479789T>C , CM000677.1:g.67479789T>C	GRCh37
NC_000015.8:g.65266843T>C	NCBI36
NG_011990.1:g.126595T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558428.6:c.511T>C	ENSP00000454165.2:p.Leu171=
ENST00000558739.2:c.781T>C	ENSP00000453684.2:p.Leu261=
ENST00000558827.2:c.511T>C	ENSP00000452767.2:p.Leu171=
ENST00000559460.6:c.781T>C	ENSP00000453082.2:p.Leu261=
ENST00000560424.2:c.1207T>C	ENSP00000455540.2:p.Leu403=
ENST00000327367.9:c.1096T>C MANE Select	ENSP00000332973.4:p.Leu366=
ENST00000679624.1:c.781T>C	ENSP00000505445.1:p.Leu261=
ENST00000680689.1:n.799T>C
ENST00000681239.1:c.781T>C	ENSP00000505641.1:p.Leu261=
ENST00000327367.8:c.1096T>C	ENSP00000332973.4:p.Leu366=
ENST00000439724.7:c.964T>C	ENSP00000401133.3:p.Leu322=
ENST00000537194.6:c.511T>C	ENSP00000445348.2:p.Leu171=
ENST00000540846.6:c.781T>C	ENSP00000437757.2:p.Leu261=
ENST00000558763.1:n.790T>C
ENST00000560402.1:n.283-5422T>C
ENST00000560424.1:c.288T>C
NM_001145102.1:c.781T>C	NP_001138574.1:p.Leu261=
NM_001145103.1:c.964T>C	NP_001138575.1:p.Leu322=
NM_001145104.1:c.511T>C	NP_001138576.1:p.Leu171=
NM_005902.3:c.1096T>C	NP_005893.1:p.Leu366=
XM_011521559.1:c.964T>C	XP_011519861.1:p.Leu322=
XM_011521560.1:c.949T>C	XP_011519862.1:p.Leu317=
XM_011521559.3:c.964T>C	XP_011519861.1:p.Leu322=
NM_005902.4:c.1096T>C MANE Select	NP_005893.1:p.Leu366=
NM_001145102.2:c.781T>C	NP_001138574.1:p.Leu261=
NM_001145103.2:c.964T>C	NP_001138575.1:p.Leu322=
NM_001145104.2:c.511T>C	NP_001138576.1:p.Leu171=