Canonical Allele Identifier: CA392958296

Gene: SMAD3

Linked Data

• MyVariant Identifiers: chr15:g.67479815G>C (hg19) ; chr15:g.67187477G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.67187477G>C , CM000677.2:g.67187477G>C	GRCh38
NC_000015.9:g.67479815G>C , CM000677.1:g.67479815G>C	GRCh37
NC_000015.8:g.65266869G>C	NCBI36
NG_011990.1:g.126621G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558428.6:c.537G>C	ENSP00000454165.2:p.Met179Ile
ENST00000558739.2:c.807G>C	ENSP00000453684.2:p.Met269Ile
ENST00000558827.2:c.537G>C	ENSP00000452767.2:p.Met179Ile
ENST00000559460.6:c.807G>C	ENSP00000453082.2:p.Met269Ile
ENST00000560424.2:c.1233G>C	ENSP00000455540.2:p.Met411Ile
ENST00000327367.9:c.1122G>C MANE Select	ENSP00000332973.4:p.Met374Ile
ENST00000679624.1:c.807G>C	ENSP00000505445.1:p.Met269Ile
ENST00000680689.1:n.825G>C
ENST00000681239.1:c.807G>C	ENSP00000505641.1:p.Met269Ile
ENST00000327367.8:c.1122G>C	ENSP00000332973.4:p.Met374Ile
ENST00000439724.7:c.990G>C	ENSP00000401133.3:p.Met330Ile
ENST00000537194.6:c.537G>C	ENSP00000445348.2:p.Met179Ile
ENST00000540846.6:c.807G>C	ENSP00000437757.2:p.Met269Ile
ENST00000558763.1:n.816G>C
ENST00000560402.1:n.283-5396G>C
ENST00000560424.1:c.314G>C
NM_001145102.1:c.807G>C	NP_001138574.1:p.Met269Ile
NM_001145103.1:c.990G>C	NP_001138575.1:p.Met330Ile
NM_001145104.1:c.537G>C	NP_001138576.1:p.Met179Ile
NM_005902.3:c.1122G>C	NP_005893.1:p.Met374Ile
XM_011521559.1:c.990G>C	XP_011519861.1:p.Met330Ile
XM_011521560.1:c.975G>C	XP_011519862.1:p.Met325Ile
XM_011521559.3:c.990G>C	XP_011519861.1:p.Met330Ile
NM_005902.4:c.1122G>C MANE Select	NP_005893.1:p.Met374Ile
NM_001145102.2:c.807G>C	NP_001138574.1:p.Met269Ile
NM_001145103.2:c.990G>C	NP_001138575.1:p.Met330Ile
NM_001145104.2:c.537G>C	NP_001138576.1:p.Met179Ile