Canonical Allele Identifier: CA392954247

Gene: SMAD3

Linked Data

• dbSNP Id: rs1962549438
• gnomAD v3: 15-67165264-G-A
• gnomAD v4: 15-67165264-G-A
• MyVariant Identifiers: chr15:g.67457602G>A (hg19) ; chr15:g.67165264G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.67165264G>A , CM000677.2:g.67165264G>A	GRCh38
NC_000015.9:g.67457602G>A , CM000677.1:g.67457602G>A	GRCh37
NC_000015.8:g.65244656G>A	NCBI36
NG_011990.1:g.104408G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558739.2:c.97G>A	ENSP00000453684.2:p.Val33Met
ENST00000559460.6:c.97G>A	ENSP00000453082.2:p.Val33Met
ENST00000560424.2:c.412G>A	ENSP00000455540.2:p.Val138Met
ENST00000327367.9:c.412G>A MANE Select	ENSP00000332973.4:p.Val138Met
ENST00000679624.1:c.97G>A	ENSP00000505445.1:p.Val33Met
ENST00000681239.1:c.97G>A	ENSP00000505641.1:p.Val33Met
ENST00000327367.8:c.412G>A	ENSP00000332973.4:p.Val138Met
ENST00000439724.7:c.280G>A	ENSP00000401133.3:p.Val94Met
ENST00000540846.6:c.97G>A	ENSP00000437757.2:p.Val33Met
ENST00000558739.1:c.97G>A	ENSP00000453684.1:p.Val33Met
ENST00000558894.5:c.97G>A	ENSP00000458060.1:p.Val33Met
ENST00000559460.5:c.97G>A	ENSP00000453082.1:p.Val33Met
ENST00000559937.1:n.262G>A
ENST00000560175.5:c.97G>A	ENSP00000455095.1:p.Val33Met
NM_001145102.1:c.97G>A	NP_001138574.1:p.Val33Met
NM_001145103.1:c.280G>A	NP_001138575.1:p.Val94Met
NM_005902.3:c.412G>A	NP_005893.1:p.Val138Met
XM_011521559.1:c.400+176G>A	XP_011519861.1:n.400+176G>A
XM_011521560.1:c.265G>A	XP_011519862.1:p.Val89Met
XM_011521559.3:c.400+176G>A	XP_011519861.1:n.400+176G>A
NM_005902.4:c.412G>A MANE Select	NP_005893.1:p.Val138Met
NM_001145102.2:c.97G>A	NP_001138574.1:p.Val33Met
NM_001145103.2:c.280G>A	NP_001138575.1:p.Val94Met