Canonical Allele Identifier: CA392954322
Gene: SMAD3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67165299G>C , CM000677.2:g.67165299G>C GRCh38
NC_000015.9:g.67457637G>C , CM000677.1:g.67457637G>C GRCh37
NC_000015.8:g.65244691G>C NCBI36
NG_011990.1:g.104443G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000558739.2:c.132G>C ENSP00000453684.2:p.Glu44Asp
ENST00000559460.6:c.132G>C ENSP00000453082.2:p.Glu44Asp
ENST00000560424.2:c.447G>C ENSP00000455540.2:p.Glu149Asp
ENST00000327367.9:c.447G>C MANE Select ENSP00000332973.4:p.Glu149Asp
ENST00000679624.1:c.132G>C ENSP00000505445.1:p.Glu44Asp
ENST00000681239.1:c.132G>C ENSP00000505641.1:p.Glu44Asp
ENST00000327367.8:c.447G>C ENSP00000332973.4:p.Glu149Asp
ENST00000439724.7:c.315G>C ENSP00000401133.3:p.Glu105Asp
ENST00000540846.6:c.132G>C ENSP00000437757.2:p.Glu44Asp
ENST00000558739.1:c.132G>C ENSP00000453684.1:p.Glu44Asp
ENST00000558894.5:c.132G>C ENSP00000458060.1:p.Glu44Asp
ENST00000559460.5:c.132G>C ENSP00000453082.1:p.Glu44Asp
ENST00000559937.1:n.297G>C
ENST00000560175.5:c.132G>C ENSP00000455095.1:p.Glu44Asp
NM_001145102.1:c.132G>C NP_001138574.1:p.Glu44Asp
NM_001145103.1:c.315G>C NP_001138575.1:p.Glu105Asp
NM_005902.3:c.447G>C NP_005893.1:p.Glu149Asp
XM_011521559.1:c.400+211G>C XP_011519861.1:n.400+211G>C
XM_011521560.1:c.300G>C XP_011519862.1:p.Glu100Asp
XM_011521559.3:c.400+211G>C XP_011519861.1:n.400+211G>C
NM_005902.4:c.447G>C MANE Select NP_005893.1:p.Glu149Asp
NM_001145102.2:c.132G>C NP_001138574.1:p.Glu44Asp
NM_001145103.2:c.315G>C NP_001138575.1:p.Glu105Asp