Canonical Allele Identifier: CA392956780

Gene: SMAD3

Linked Data

• MyVariant Identifiers: chr15:g.67477092G>T (hg19) ; chr15:g.67184754G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.67184754G>T , CM000677.2:g.67184754G>T	GRCh38
NC_000015.9:g.67477092G>T , CM000677.1:g.67477092G>T	GRCh37
NC_000015.8:g.65264146G>T	NCBI36
NG_011990.1:g.123898G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558428.6:c.314G>T	ENSP00000454165.2:p.Gly105Val
ENST00000558739.2:c.584G>T	ENSP00000453684.2:p.Gly195Val
ENST00000558827.2:c.314G>T	ENSP00000452767.2:p.Gly105Val
ENST00000559460.6:c.584G>T	ENSP00000453082.2:p.Gly195Val
ENST00000560424.2:c.899G>T	ENSP00000455540.2:p.Gly300Val
ENST00000327367.9:c.899G>T MANE Select	ENSP00000332973.4:p.Gly300Val
ENST00000679624.1:c.584G>T	ENSP00000505445.1:p.Gly195Val
ENST00000680689.1:n.602G>T
ENST00000681239.1:c.584G>T	ENSP00000505641.1:p.Gly195Val
ENST00000327367.8:c.899G>T	ENSP00000332973.4:p.Gly300Val
ENST00000439724.7:c.767G>T	ENSP00000401133.3:p.Gly256Val
ENST00000537194.6:c.314G>T	ENSP00000445348.2:p.Gly105Val
ENST00000540846.6:c.584G>T	ENSP00000437757.2:p.Gly195Val
ENST00000558827.1:c.314G>T	ENSP00000452767.1:p.Gly105Val
ENST00000558894.5:c.557-2611G>T	ENSP00000458060.1:n.557-2611G>T
ENST00000560402.1:n.283-8119G>T
NM_001145102.1:c.584G>T	NP_001138574.1:p.Gly195Val
NM_001145103.1:c.767G>T	NP_001138575.1:p.Gly256Val
NM_001145104.1:c.314G>T	NP_001138576.1:p.Gly105Val
NM_005902.3:c.899G>T	NP_005893.1:p.Gly300Val
XM_011521559.1:c.767G>T	XP_011519861.1:p.Gly256Val
XM_011521560.1:c.752G>T	XP_011519862.1:p.Gly251Val
XM_011521559.3:c.767G>T	XP_011519861.1:p.Gly256Val
NM_005902.4:c.899G>T MANE Select	NP_005893.1:p.Gly300Val
NM_001145102.2:c.584G>T	NP_001138574.1:p.Gly195Val
NM_001145103.2:c.767G>T	NP_001138575.1:p.Gly256Val
NM_001145104.2:c.314G>T	NP_001138576.1:p.Gly105Val