Canonical Allele Identifier: CA392957371
Gene: SMAD3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67184858C>T , CM000677.2:g.67184858C>T GRCh38
NC_000015.9:g.67477196C>T , CM000677.1:g.67477196C>T GRCh37
NC_000015.8:g.65264250C>T NCBI36
NG_011990.1:g.124002C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000558428.6:c.418C>T ENSP00000454165.2:p.Pro140Ser
ENST00000558739.2:c.688C>T ENSP00000453684.2:p.Pro230Ser
ENST00000558827.2:c.418C>T ENSP00000452767.2:p.Pro140Ser
ENST00000559460.6:c.688C>T ENSP00000453082.2:p.Pro230Ser
ENST00000560424.2:c.1003C>T ENSP00000455540.2:p.Pro335Ser
ENST00000327367.9:c.1003C>T MANE Select ENSP00000332973.4:p.Pro335Ser
ENST00000679624.1:c.688C>T ENSP00000505445.1:p.Pro230Ser
ENST00000680689.1:n.706C>T
ENST00000681239.1:c.688C>T ENSP00000505641.1:p.Pro230Ser
ENST00000327367.8:c.1003C>T ENSP00000332973.4:p.Pro335Ser
ENST00000439724.7:c.871C>T ENSP00000401133.3:p.Pro291Ser
ENST00000537194.6:c.418C>T ENSP00000445348.2:p.Pro140Ser
ENST00000540846.6:c.688C>T ENSP00000437757.2:p.Pro230Ser
ENST00000558894.5:c.557-2507C>T ENSP00000458060.1:n.557-2507C>T
ENST00000560402.1:n.283-8015C>T
ENST00000560424.1:c.84C>T
NM_001145102.1:c.688C>T NP_001138574.1:p.Pro230Ser
NM_001145103.1:c.871C>T NP_001138575.1:p.Pro291Ser
NM_001145104.1:c.418C>T NP_001138576.1:p.Pro140Ser
NM_005902.3:c.1003C>T NP_005893.1:p.Pro335Ser
XM_011521559.1:c.871C>T XP_011519861.1:p.Pro291Ser
XM_011521560.1:c.856C>T XP_011519862.1:p.Pro286Ser
XM_011521559.3:c.871C>T XP_011519861.1:p.Pro291Ser
NM_005902.4:c.1003C>T MANE Select NP_005893.1:p.Pro335Ser
NM_001145102.2:c.688C>T NP_001138574.1:p.Pro230Ser
NM_001145103.2:c.871C>T NP_001138575.1:p.Pro291Ser
NM_001145104.2:c.418C>T NP_001138576.1:p.Pro140Ser