Canonical Allele Identifier: CA2084883487
Gene: SMAD9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.36879320_36879324delinsCTTCT , CM000675.2:g.36879320_36879324delinsCTTCT GRCh38
NC_000013.10:g.37453457_37453461delinsCTTCT , CM000675.1:g.37453457_37453461delinsCTTCT GRCh37
NC_000013.9:g.36351457_36351461delinsCTTCT NCBI36
NG_016963.1:g.45949_45953delinsAGAAG , LRG_703:g.45949_45953delinsAGAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000350148.10:c.366_370delinsAGAAG ENSP00000239885.6:p.Lys122=
ENST00000379826.5:c.366_370delinsAGAAG MANE Select ENSP00000369154.4:p.Lys122=
ENST00000399275.7:c.366_370delinsAGAAG ENSP00000382216.3:p.Lys122=
ENST00000350148.9:c.366_370delinsAGAAG ENSP00000239885.6:p.Lys122=
ENST00000379826.4:c.366_370delinsAGAAG ENSP00000369154.4:p.Lys122=
ENST00000399275.6:c.366_370delinsAGAAG ENSP00000382216.2:p.Lys122=
NM_001127217.2:c.366_370delinsAGAAG , LRG_703t1:c.366_370delinsAGAAG NP_001120689.1:p.Lys122=
NM_005905.5:c.366_370delinsAGAAG NP_005896.1:p.Lys122=
XM_005266401.2:c.366_370delinsAGAAG XP_005266458.1:p.Lys122=
XM_005266403.2:c.366_370delinsAGAAG XP_005266460.1:p.Lys122=
XM_005266404.2:c.366_370delinsAGAAG XP_005266461.1:p.Lys122=
XM_006719827.2:c.366_370delinsAGAAG XP_006719890.1:p.Lys122=
XM_011535096.1:c.366_370delinsAGAAG XP_011533398.1:p.Lys122=
XM_005266401.3:c.366_370delinsAGAAG XP_005266458.1:p.Lys122=
XM_005266403.3:c.366_370delinsAGAAG XP_005266460.1:p.Lys122=
XM_005266404.3:c.366_370delinsAGAAG XP_005266461.1:p.Lys122=
XM_006719827.3:c.366_370delinsAGAAG XP_006719890.1:p.Lys122=
NM_001127217.3:c.366_370delinsAGAAG MANE Select NP_001120689.1:p.Lys122=
NM_005905.6:c.366_370delinsAGAAG NP_005896.1:p.Lys122=
NM_001378621.1:c.366_370delinsAGAAG NP_001365550.1:p.Lys122=