Canonical Allele Identifier: CA392957224

Gene: SMAD3

Linked Data

• dbSNP Id: rs2140320113
• MyVariant Identifiers: chr15:g.67477171G>A (hg19) ; chr15:g.67184833G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.67184833G>A , CM000677.2:g.67184833G>A	GRCh38
NC_000015.9:g.67477171G>A , CM000677.1:g.67477171G>A	GRCh37
NC_000015.8:g.65264225G>A	NCBI36
NG_011990.1:g.123977G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558428.6:c.393G>A	ENSP00000454165.2:p.Trp131Ter
ENST00000558739.2:c.663G>A	ENSP00000453684.2:p.Trp221Ter
ENST00000558827.2:c.393G>A	ENSP00000452767.2:p.Trp131Ter
ENST00000559460.6:c.663G>A	ENSP00000453082.2:p.Trp221Ter
ENST00000560424.2:c.978G>A	ENSP00000455540.2:p.Trp326Ter
ENST00000327367.9:c.978G>A MANE Select	ENSP00000332973.4:p.Trp326Ter
ENST00000679624.1:c.663G>A	ENSP00000505445.1:p.Trp221Ter
ENST00000680689.1:n.681G>A
ENST00000681239.1:c.663G>A	ENSP00000505641.1:p.Trp221Ter
ENST00000327367.8:c.978G>A	ENSP00000332973.4:p.Trp326Ter
ENST00000439724.7:c.846G>A	ENSP00000401133.3:p.Trp282Ter
ENST00000537194.6:c.393G>A	ENSP00000445348.2:p.Trp131Ter
ENST00000540846.6:c.663G>A	ENSP00000437757.2:p.Trp221Ter
ENST00000558894.5:c.557-2532G>A	ENSP00000458060.1:n.557-2532G>A
ENST00000560402.1:n.283-8040G>A
ENST00000560424.1:c.59G>A
NM_001145102.1:c.663G>A	NP_001138574.1:p.Trp221Ter
NM_001145103.1:c.846G>A	NP_001138575.1:p.Trp282Ter
NM_001145104.1:c.393G>A	NP_001138576.1:p.Trp131Ter
NM_005902.3:c.978G>A	NP_005893.1:p.Trp326Ter
XM_011521559.1:c.846G>A	XP_011519861.1:p.Trp282Ter
XM_011521560.1:c.831G>A	XP_011519862.1:p.Trp277Ter
XM_011521559.3:c.846G>A	XP_011519861.1:p.Trp282Ter
NM_005902.4:c.978G>A MANE Select	NP_005893.1:p.Trp326Ter
NM_001145102.2:c.663G>A	NP_001138574.1:p.Trp221Ter
NM_001145103.2:c.846G>A	NP_001138575.1:p.Trp282Ter
NM_001145104.2:c.393G>A	NP_001138576.1:p.Trp131Ter