Canonical Allele Identifier: CA387853342
Gene: SMAD9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.36879533C>G , CM000675.2:g.36879533C>G GRCh38
NC_000013.10:g.37453670C>G , CM000675.1:g.37453670C>G GRCh37
NC_000013.9:g.36351670C>G NCBI36
NG_016963.1:g.45740G>C , LRG_703:g.45740G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000483941.2:n.596G>C
ENST00000350148.10:c.157G>C ENSP00000239885.6:p.Asp53His
ENST00000379826.5:c.157G>C MANE Select ENSP00000369154.4:p.Asp53His
ENST00000399275.7:c.157G>C ENSP00000382216.3:p.Asp53His
ENST00000350148.9:c.157G>C ENSP00000239885.6:p.Asp53His
ENST00000379826.4:c.157G>C ENSP00000369154.4:p.Asp53His
ENST00000399275.6:c.157G>C ENSP00000382216.2:p.Asp53His
ENST00000483941.1:n.474G>C
NM_001127217.2:c.157G>C , LRG_703t1:c.157G>C NP_001120689.1:p.Asp53His
NM_005905.5:c.157G>C NP_005896.1:p.Asp53His
XM_005266401.2:c.157G>C XP_005266458.1:p.Asp53His
XM_005266403.2:c.157G>C XP_005266460.1:p.Asp53His
XM_005266404.2:c.157G>C XP_005266461.1:p.Asp53His
XM_006719827.2:c.157G>C XP_006719890.1:p.Asp53His
XM_011535096.1:c.157G>C XP_011533398.1:p.Asp53His
XM_005266401.3:c.157G>C XP_005266458.1:p.Asp53His
XM_005266403.3:c.157G>C XP_005266460.1:p.Asp53His
XM_005266404.3:c.157G>C XP_005266461.1:p.Asp53His
XM_006719827.3:c.157G>C XP_006719890.1:p.Asp53His
NM_001127217.3:c.157G>C MANE Select NP_001120689.1:p.Asp53His
NM_005905.6:c.157G>C NP_005896.1:p.Asp53His
NM_001378621.1:c.157G>C NP_001365550.1:p.Asp53His