Canonical Allele Identifier: CA392958362
Gene: SMAD3 HGNC NCBI

Linked Data

dbSNP Id: rs2140323802

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.67187505T>A , CM000677.2:g.67187505T>A GRCh38
NC_000015.9:g.67479843T>A , CM000677.1:g.67479843T>A GRCh37
NC_000015.8:g.65266897T>A NCBI36
NG_011990.1:g.126649T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000558428.6:c.565T>A ENSP00000454165.2:p.Tyr189Asn
ENST00000558739.2:c.835T>A ENSP00000453684.2:p.Tyr279Asn
ENST00000558827.2:c.565T>A ENSP00000452767.2:p.Tyr189Asn
ENST00000559460.6:c.835T>A ENSP00000453082.2:p.Tyr279Asn
ENST00000560424.2:c.1261T>A ENSP00000455540.2:p.Tyr421Asn
ENST00000327367.9:c.1150T>A MANE Select ENSP00000332973.4:p.Tyr384Asn
ENST00000679624.1:c.835T>A ENSP00000505445.1:p.Tyr279Asn
ENST00000680689.1:n.853T>A
ENST00000681239.1:c.835T>A ENSP00000505641.1:p.Tyr279Asn
ENST00000327367.8:c.1150T>A ENSP00000332973.4:p.Tyr384Asn
ENST00000439724.7:c.1018T>A ENSP00000401133.3:p.Tyr340Asn
ENST00000537194.6:c.565T>A ENSP00000445348.2:p.Tyr189Asn
ENST00000540846.6:c.835T>A ENSP00000437757.2:p.Tyr279Asn
ENST00000558763.1:n.844T>A
ENST00000560402.1:n.283-5368T>A
ENST00000560424.1:c.342T>A
NM_001145102.1:c.835T>A NP_001138574.1:p.Tyr279Asn
NM_001145103.1:c.1018T>A NP_001138575.1:p.Tyr340Asn
NM_001145104.1:c.565T>A NP_001138576.1:p.Tyr189Asn
NM_005902.3:c.1150T>A NP_005893.1:p.Tyr384Asn
XM_011521559.1:c.1018T>A XP_011519861.1:p.Tyr340Asn
XM_011521560.1:c.1003T>A XP_011519862.1:p.Tyr335Asn
XM_011521559.3:c.1018T>A XP_011519861.1:p.Tyr340Asn
NM_005902.4:c.1150T>A MANE Select NP_005893.1:p.Tyr384Asn
NM_001145102.2:c.835T>A NP_001138574.1:p.Tyr279Asn
NM_001145103.2:c.1018T>A NP_001138575.1:p.Tyr340Asn
NM_001145104.2:c.565T>A NP_001138576.1:p.Tyr189Asn