Canonical Allele Identifier: CA392954092
Gene: SMAD3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67165035A>C , CM000677.2:g.67165035A>C GRCh38
NC_000015.9:g.67457373A>C , CM000677.1:g.67457373A>C GRCh37
NC_000015.8:g.65244427A>C NCBI36
NG_011990.1:g.104179A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000558739.2:c.32A>C ENSP00000453684.2:p.Lys11Thr
ENST00000559460.6:c.32A>C ENSP00000453082.2:p.Lys11Thr
ENST00000560424.2:c.347A>C ENSP00000455540.2:p.Lys116Thr
ENST00000327367.9:c.347A>C MANE Select ENSP00000332973.4:p.Lys116Thr
ENST00000679624.1:c.32A>C ENSP00000505445.1:p.Lys11Thr
ENST00000681239.1:c.32A>C ENSP00000505641.1:p.Lys11Thr
ENST00000327367.8:c.347A>C ENSP00000332973.4:p.Lys116Thr
ENST00000439724.7:c.215A>C ENSP00000401133.3:p.Lys72Thr
ENST00000540846.6:c.32A>C ENSP00000437757.2:p.Lys11Thr
ENST00000558739.1:c.32A>C ENSP00000453684.1:p.Lys11Thr
ENST00000558894.5:c.32A>C ENSP00000458060.1:p.Lys11Thr
ENST00000559092.1:c.*1A>C ENSP00000453788.1:n.*1A>C
ENST00000559460.5:c.32A>C ENSP00000453082.1:p.Lys11Thr
ENST00000559937.1:n.197A>C
ENST00000560175.5:c.32A>C ENSP00000455095.1:p.Lys11Thr
NM_001145102.1:c.32A>C NP_001138574.1:p.Lys11Thr
NM_001145103.1:c.215A>C NP_001138575.1:p.Lys72Thr
NM_005902.3:c.347A>C NP_005893.1:p.Lys116Thr
XM_011521559.1:c.347A>C XP_011519861.1:p.Lys116Thr
XM_011521560.1:c.200A>C XP_011519862.1:p.Lys67Thr
XM_011521559.3:c.347A>C XP_011519861.1:p.Lys116Thr
NM_005902.4:c.347A>C MANE Select NP_005893.1:p.Lys116Thr
NM_001145102.2:c.32A>C NP_001138574.1:p.Lys11Thr
NM_001145103.2:c.215A>C NP_001138575.1:p.Lys72Thr