Canonical Allele Identifier: CA2184410302
Gene: SMAD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67164898C= , CM000677.2:g.67164898C= GRCh38
NC_000015.9:g.67457236C= , CM000677.1:g.67457236C= GRCh37
NC_000015.8:g.65244290C= NCBI36
NG_011990.1:g.104042C=

Transcript Alleles

HGVS Amino-acid change
ENST00000558739.2:c.-106C= ENSP00000453684.2:n.-106C=
ENST00000559460.6:c.-106C= ENSP00000453082.2:n.-106C=
ENST00000560424.2:c.210C= ENSP00000455540.2:p.Ser70=
ENST00000327367.9:c.210C= MANE Select ENSP00000332973.4:p.Ser70=
ENST00000679624.1:c.-106C= ENSP00000505445.1:n.-106C=
ENST00000681239.1:c.-106C= ENSP00000505641.1:n.-106C=
ENST00000327367.8:c.210C= ENSP00000332973.4:p.Ser70=
ENST00000439724.7:c.78C= ENSP00000401133.3:p.Ser26=
ENST00000540846.6:c.-106C= ENSP00000437757.2:n.-106C=
ENST00000558739.1:c.-106C= ENSP00000453684.1:n.-106C=
ENST00000558894.5:c.-106C= ENSP00000458060.1:n.-106C=
ENST00000559092.1:c.155C= ENSP00000453788.1:p.Pro52=
ENST00000559460.5:c.-106C= ENSP00000453082.1:n.-106C=
ENST00000559937.1:n.60C=
ENST00000560175.5:c.-106C= ENSP00000455095.1:n.-106C=
NM_001145102.1:c.-106C= NP_001138574.1:n.-106C=
NM_001145103.1:c.78C= NP_001138575.1:p.Ser26=
NM_005902.3:c.210C= NP_005893.1:p.Ser70=
XM_011521559.1:c.210C= XP_011519861.1:p.Ser70=
XM_011521560.1:c.63C= XP_011519862.1:p.Ser21=
XM_011521559.3:c.210C= XP_011519861.1:p.Ser70=
NM_005902.4:c.210C= MANE Select NP_005893.1:p.Ser70=
NM_001145102.2:c.-106C= NP_001138574.1:n.-106C=
NM_001145103.2:c.78C= NP_001138575.1:p.Ser26=