Canonical Allele Identifier: CA392958201
Gene: SMAD3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67187433T>C , CM000677.2:g.67187433T>C GRCh38
NC_000015.9:g.67479771T>C , CM000677.1:g.67479771T>C GRCh37
NC_000015.8:g.65266825T>C NCBI36
NG_011990.1:g.126577T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000558428.6:c.493T>C ENSP00000454165.2:p.Phe165Leu
ENST00000558739.2:c.763T>C ENSP00000453684.2:p.Phe255Leu
ENST00000558827.2:c.493T>C ENSP00000452767.2:p.Phe165Leu
ENST00000559460.6:c.763T>C ENSP00000453082.2:p.Phe255Leu
ENST00000560424.2:c.1189T>C ENSP00000455540.2:p.Phe397Leu
ENST00000327367.9:c.1078T>C MANE Select ENSP00000332973.4:p.Phe360Leu
ENST00000679624.1:c.763T>C ENSP00000505445.1:p.Phe255Leu
ENST00000680689.1:n.781T>C
ENST00000681239.1:c.763T>C ENSP00000505641.1:p.Phe255Leu
ENST00000327367.8:c.1078T>C ENSP00000332973.4:p.Phe360Leu
ENST00000439724.7:c.946T>C ENSP00000401133.3:p.Phe316Leu
ENST00000537194.6:c.493T>C ENSP00000445348.2:p.Phe165Leu
ENST00000540846.6:c.763T>C ENSP00000437757.2:p.Phe255Leu
ENST00000558763.1:n.772T>C
ENST00000558894.5:c.625T>C ENSP00000458060.1:p.Phe209Leu
ENST00000560402.1:n.283-5440T>C
ENST00000560424.1:c.270T>C
NM_001145102.1:c.763T>C NP_001138574.1:p.Phe255Leu
NM_001145103.1:c.946T>C NP_001138575.1:p.Phe316Leu
NM_001145104.1:c.493T>C NP_001138576.1:p.Phe165Leu
NM_005902.3:c.1078T>C NP_005893.1:p.Phe360Leu
XM_011521559.1:c.946T>C XP_011519861.1:p.Phe316Leu
XM_011521560.1:c.931T>C XP_011519862.1:p.Phe311Leu
XM_011521559.3:c.946T>C XP_011519861.1:p.Phe316Leu
NM_005902.4:c.1078T>C MANE Select NP_005893.1:p.Phe360Leu
NM_001145102.2:c.763T>C NP_001138574.1:p.Phe255Leu
NM_001145103.2:c.946T>C NP_001138575.1:p.Phe316Leu
NM_001145104.2:c.493T>C NP_001138576.1:p.Phe165Leu