Canonical Allele Identifier: CA321543

Gene: SMAD3

Linked Data

• ClinVar Variation Id: 213804
• ClinVar RCV Id: RCV000197105 ; RCV001525711 ; RCV003996914
• dbSNP Id: rs863223767
• gnomAD v2: 15-67457591-T-C
• gnomAD v4: 15-67165253-T-C
• MyVariant Identifiers: chr15:g.67457591T>C (hg19) ; chr15:g.67165253T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.67165253T>C , CM000677.2:g.67165253T>C	GRCh38
NC_000015.9:g.67457591T>C , CM000677.1:g.67457591T>C	GRCh37
NC_000015.8:g.65244645T>C	NCBI36
NG_011990.1:g.104397T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558739.2:c.86T>C	ENSP00000453684.2:p.Val29Ala
ENST00000559460.6:c.86T>C	ENSP00000453082.2:p.Val29Ala
ENST00000560424.2:c.401T>C	ENSP00000455540.2:p.Val134Ala
ENST00000327367.9:c.401T>C MANE Select	ENSP00000332973.4:p.Val134Ala
ENST00000679624.1:c.86T>C	ENSP00000505445.1:p.Val29Ala
ENST00000681239.1:c.86T>C	ENSP00000505641.1:p.Val29Ala
ENST00000327367.8:c.401T>C	ENSP00000332973.4:p.Val134Ala
ENST00000439724.7:c.269T>C	ENSP00000401133.3:p.Val90Ala
ENST00000540846.6:c.86T>C	ENSP00000437757.2:p.Val29Ala
ENST00000558739.1:c.86T>C	ENSP00000453684.1:p.Val29Ala
ENST00000558894.5:c.86T>C	ENSP00000458060.1:p.Val29Ala
ENST00000559460.5:c.86T>C	ENSP00000453082.1:p.Val29Ala
ENST00000559937.1:n.251T>C
ENST00000560175.5:c.86T>C	ENSP00000455095.1:p.Val29Ala
NM_001145102.1:c.86T>C	NP_001138574.1:p.Val29Ala
NM_001145103.1:c.269T>C	NP_001138575.1:p.Val90Ala
NM_005902.3:c.401T>C	NP_005893.1:p.Val134Ala
XM_011521559.1:c.400+165T>C	XP_011519861.1:n.400+165T>C
XM_011521560.1:c.254T>C	XP_011519862.1:p.Val85Ala
XM_011521559.3:c.400+165T>C	XP_011519861.1:n.400+165T>C
NM_005902.4:c.401T>C MANE Select	NP_005893.1:p.Val134Ala
NM_001145102.2:c.86T>C	NP_001138574.1:p.Val29Ala
NM_001145103.2:c.269T>C	NP_001138575.1:p.Val90Ala