Canonical Allele Identifier: CA392954297
Gene: SMAD3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67165287G>T , CM000677.2:g.67165287G>T GRCh38
NC_000015.9:g.67457625G>T , CM000677.1:g.67457625G>T GRCh37
NC_000015.8:g.65244679G>T NCBI36
NG_011990.1:g.104431G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000558739.2:c.120G>T ENSP00000453684.2:p.Glu40Asp
ENST00000559460.6:c.120G>T ENSP00000453082.2:p.Glu40Asp
ENST00000560424.2:c.435G>T ENSP00000455540.2:p.Glu145Asp
ENST00000327367.9:c.435G>T MANE Select ENSP00000332973.4:p.Glu145Asp
ENST00000679624.1:c.120G>T ENSP00000505445.1:p.Glu40Asp
ENST00000681239.1:c.120G>T ENSP00000505641.1:p.Glu40Asp
ENST00000327367.8:c.435G>T ENSP00000332973.4:p.Glu145Asp
ENST00000439724.7:c.303G>T ENSP00000401133.3:p.Glu101Asp
ENST00000540846.6:c.120G>T ENSP00000437757.2:p.Glu40Asp
ENST00000558739.1:c.120G>T ENSP00000453684.1:p.Glu40Asp
ENST00000558894.5:c.120G>T ENSP00000458060.1:p.Glu40Asp
ENST00000559460.5:c.120G>T ENSP00000453082.1:p.Glu40Asp
ENST00000559937.1:n.285G>T
ENST00000560175.5:c.120G>T ENSP00000455095.1:p.Glu40Asp
NM_001145102.1:c.120G>T NP_001138574.1:p.Glu40Asp
NM_001145103.1:c.303G>T NP_001138575.1:p.Glu101Asp
NM_005902.3:c.435G>T NP_005893.1:p.Glu145Asp
XM_011521559.1:c.400+199G>T XP_011519861.1:n.400+199G>T
XM_011521560.1:c.288G>T XP_011519862.1:p.Glu96Asp
XM_011521559.3:c.400+199G>T XP_011519861.1:n.400+199G>T
NM_005902.4:c.435G>T MANE Select NP_005893.1:p.Glu145Asp
NM_001145102.2:c.120G>T NP_001138574.1:p.Glu40Asp
NM_001145103.2:c.303G>T NP_001138575.1:p.Glu101Asp