Canonical Allele Identifier: CA970971082
Gene: SMAD3 HGNC NCBI

Linked Data

dbSNP Id: rs1963256495

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67187624del , CM000677.2:g.67187624del GRCh38
NC_000015.9:g.67479962del , CM000677.1:g.67479962del GRCh37
NC_000015.8:g.65267016del NCBI36
NG_011990.1:g.126768del

Transcript Alleles

HGVS Amino-acid Change
ENST00000558428.6:c.569+115del ENSP00000454165.2:n.569+115del
ENST00000558739.2:c.839+115del ENSP00000453684.2:n.839+115del
ENST00000558827.2:c.569+115del ENSP00000452767.2:n.569+115del
ENST00000559460.6:c.839+115del ENSP00000453082.2:n.839+115del
ENST00000560424.2:c.1265+115del ENSP00000455540.2:n.1265+115del
ENST00000327367.9:c.1154+115del MANE Select ENSP00000332973.4:n.1154+115del
ENST00000679624.1:c.839+115del ENSP00000505445.1:n.839+115del
ENST00000680689.1:n.857+115del
ENST00000681239.1:c.839+115del ENSP00000505641.1:n.839+115del
ENST00000327367.8:c.1154+115del ENSP00000332973.4:n.1154+115del
ENST00000439724.7:c.1022+115del ENSP00000401133.3:n.1022+115del
ENST00000537194.6:c.569+115del ENSP00000445348.2:n.569+115del
ENST00000540846.6:c.839+115del ENSP00000437757.2:n.839+115del
ENST00000558763.1:n.848+115del
ENST00000560402.1:n.283-5249del
ENST00000560424.1:c.346+115del
NM_001145102.1:c.839+115del NP_001138574.1:n.839+115del
NM_001145103.1:c.1022+115del NP_001138575.1:n.1022+115del
NM_001145104.1:c.569+115del NP_001138576.1:n.569+115del
NM_005902.3:c.1154+115del NP_005893.1:n.1154+115del
XM_011521559.1:c.1022+115del XP_011519861.1:n.1022+115del
XM_011521560.1:c.1007+115del XP_011519862.1:n.1007+115del
XM_011521559.3:c.1022+115del XP_011519861.1:n.1022+115del
NM_005902.4:c.1154+115del MANE Select NP_005893.1:n.1154+115del
NM_001145102.2:c.839+115del NP_001138574.1:n.839+115del
NM_001145103.2:c.1022+115del NP_001138575.1:n.1022+115del
NM_001145104.2:c.569+115del NP_001138576.1:n.569+115del