Canonical Allele Identifier: CA2184423366
Gene: SMAD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67192745_67192747delinsCTT , CM000677.2:g.67192745_67192747delinsCTT GRCh38
NC_000015.9:g.67485083_67485085delinsCTT , CM000677.1:g.67485083_67485085delinsCTT GRCh37
NC_000015.8:g.65272137_65272139delinsCTT NCBI36
NG_011990.1:g.131889_131891delinsCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000558739.2:c.*2209_*2211delinsCTT ENSP00000453684.2:n.*2209_*2211delinsCTT
ENST00000559460.6:c.*2209_*2211delinsCTT ENSP00000453082.2:n.*2209_*2211delinsCTT
ENST00000327367.9:c.*2209_*2211delinsCTT MANE Select ENSP00000332973.4:n.*2209_*2211delinsCTT
ENST00000679624.1:c.*2209_*2211delinsCTT ENSP00000505445.1:n.*2209_*2211delinsCTT
ENST00000681239.1:c.*2209_*2211delinsCTT ENSP00000505641.1:n.*2209_*2211delinsCTT
ENST00000327367.8:c.*2209_*2211delinsCTT ENSP00000332973.4:n.*2209_*2211delinsCTT
ENST00000560402.1:n.283-128_283-126delinsCTT
NM_001145102.1:c.*2209_*2211delinsCTT NP_001138574.1:n.*2209_*2211delinsCTT
NM_001145103.1:c.*2209_*2211delinsCTT NP_001138575.1:n.*2209_*2211delinsCTT
NM_001145104.1:c.*2209_*2211delinsCTT NP_001138576.1:n.*2209_*2211delinsCTT
NM_005902.3:c.*2209_*2211delinsCTT NP_005893.1:n.*2209_*2211delinsCTT
XM_011521559.1:c.*2209_*2211delinsCTT XP_011519861.1:n.*2209_*2211delinsCTT
XM_011521560.1:c.*2209_*2211delinsCTT XP_011519862.1:n.*2209_*2211delinsCTT
XM_011521559.3:c.*2209_*2211delinsCTT XP_011519861.1:n.*2209_*2211delinsCTT
NM_005902.4:c.*2209_*2211delinsCTT MANE Select NP_005893.1:n.*2209_*2211delinsCTT
NM_001145102.2:c.*2209_*2211delinsCTT NP_001138574.1:n.*2209_*2211delinsCTT
NM_001145103.2:c.*2209_*2211delinsCTT NP_001138575.1:n.*2209_*2211delinsCTT
NM_001145104.2:c.*2209_*2211delinsCTT NP_001138576.1:n.*2209_*2211delinsCTT