Canonical Allele Identifier: CA490916613

Gene: SMAD3

Linked Data

• MyVariant Identifiers: chr15:g.67477186C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.67184848C>G , CM000677.2:g.67184848C>G	GRCh38
NC_000015.9:g.67477186C>G , CM000677.1:g.67477186C>G	GRCh37
NC_000015.8:g.65264240C>G	NCBI36
NG_011990.1:g.123992C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558428.6:c.408C>G	ENSP00000454165.2:p.Val136=
ENST00000558739.2:c.678C>G	ENSP00000453684.2:p.Val226=
ENST00000558827.2:c.408C>G	ENSP00000452767.2:p.Val136=
ENST00000559460.6:c.678C>G	ENSP00000453082.2:p.Val226=
ENST00000560424.2:c.993C>G	ENSP00000455540.2:p.Val331=
ENST00000327367.9:c.993C>G MANE Select	ENSP00000332973.4:p.Val331=
ENST00000679624.1:c.678C>G	ENSP00000505445.1:p.Val226=
ENST00000680689.1:n.696C>G
ENST00000681239.1:c.678C>G	ENSP00000505641.1:p.Val226=
ENST00000327367.8:c.993C>G	ENSP00000332973.4:p.Val331=
ENST00000439724.7:c.861C>G	ENSP00000401133.3:p.Val287=
ENST00000537194.6:c.408C>G	ENSP00000445348.2:p.Val136=
ENST00000540846.6:c.678C>G	ENSP00000437757.2:p.Val226=
ENST00000558894.5:c.557-2517C>G	ENSP00000458060.1:n.557-2517C>G
ENST00000560402.1:n.283-8025C>G
ENST00000560424.1:c.74C>G
NM_001145102.1:c.678C>G	NP_001138574.1:p.Val226=
NM_001145103.1:c.861C>G	NP_001138575.1:p.Val287=
NM_001145104.1:c.408C>G	NP_001138576.1:p.Val136=
NM_005902.3:c.993C>G	NP_005893.1:p.Val331=
XM_011521559.1:c.861C>G	XP_011519861.1:p.Val287=
XM_011521560.1:c.846C>G	XP_011519862.1:p.Val282=
XM_011521559.3:c.861C>G	XP_011519861.1:p.Val287=
NM_005902.4:c.993C>G MANE Select	NP_005893.1:p.Val331=
NM_001145102.2:c.678C>G	NP_001138574.1:p.Val226=
NM_001145103.2:c.861C>G	NP_001138575.1:p.Val287=
NM_001145104.2:c.408C>G	NP_001138576.1:p.Val136=