Canonical Allele Identifier: CA16614720

Gene: SMAD3

Linked Data

• ClinVar Variation Id: 405562
• ClinVar RCV Id: RCV000476466
• dbSNP Id: rs1060500767
• MyVariant Identifiers: chr15:g.67477100G>A (hg19) ; chr15:g.67184762G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.67184762G>A , CM000677.2:g.67184762G>A	GRCh38
NC_000015.9:g.67477100G>A , CM000677.1:g.67477100G>A	GRCh37
NC_000015.8:g.65264154G>A	NCBI36
NG_011990.1:g.123906G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558428.6:c.322G>A	ENSP00000454165.2:p.Val108Ile
ENST00000558739.2:c.592G>A	ENSP00000453684.2:p.Val198Ile
ENST00000558827.2:c.322G>A	ENSP00000452767.2:p.Val108Ile
ENST00000559460.6:c.592G>A	ENSP00000453082.2:p.Val198Ile
ENST00000560424.2:c.907G>A	ENSP00000455540.2:p.Val303Ile
ENST00000327367.9:c.907G>A MANE Select	ENSP00000332973.4:p.Val303Ile
ENST00000679624.1:c.592G>A	ENSP00000505445.1:p.Val198Ile
ENST00000680689.1:n.610G>A
ENST00000681239.1:c.592G>A	ENSP00000505641.1:p.Val198Ile
ENST00000327367.8:c.907G>A	ENSP00000332973.4:p.Val303Ile
ENST00000439724.7:c.775G>A	ENSP00000401133.3:p.Val259Ile
ENST00000537194.6:c.322G>A	ENSP00000445348.2:p.Val108Ile
ENST00000540846.6:c.592G>A	ENSP00000437757.2:p.Val198Ile
ENST00000558827.1:c.322G>A	ENSP00000452767.1:p.Val108Ile
ENST00000558894.5:c.557-2603G>A	ENSP00000458060.1:n.557-2603G>A
ENST00000560402.1:n.283-8111G>A
NM_001145102.1:c.592G>A	NP_001138574.1:p.Val198Ile
NM_001145103.1:c.775G>A	NP_001138575.1:p.Val259Ile
NM_001145104.1:c.322G>A	NP_001138576.1:p.Val108Ile
NM_005902.3:c.907G>A	NP_005893.1:p.Val303Ile
XM_011521559.1:c.775G>A	XP_011519861.1:p.Val259Ile
XM_011521560.1:c.760G>A	XP_011519862.1:p.Val254Ile
XM_011521559.3:c.775G>A	XP_011519861.1:p.Val259Ile
NM_005902.4:c.907G>A MANE Select	NP_005893.1:p.Val303Ile
NM_001145102.2:c.592G>A	NP_001138574.1:p.Val198Ile
NM_001145103.2:c.775G>A	NP_001138575.1:p.Val259Ile
NM_001145104.2:c.322G>A	NP_001138576.1:p.Val108Ile