Canonical Allele Identifier: CA2641839455
Gene: SMAD4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.51078533T>A , CM000680.2:g.51078533T>A GRCh38
NC_000018.9:g.48604903T>A , CM000680.1:g.48604903T>A GRCh37
NC_000018.8:g.46858901T>A NCBI36
NG_013013.2:g.115494T>A , LRG_318:g.115494T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000588860.6:c.*66T>A ENSP00000465878.2:n.*66T>A
ENST00000589076.6:c.*66T>A ENSP00000466934.2:n.*66T>A
ENST00000589941.2:c.*66T>A ENSP00000465874.2:n.*66T>A
ENST00000590061.2:c.*66T>A ENSP00000464772.2:n.*66T>A
ENST00000593223.2:c.*1722T>A ENSP00000466118.2:n.*1722T>A
ENST00000611848.2:c.*377T>A ENSP00000478613.2:n.*377T>A
ENST00000684953.1:n.3740T>A
ENST00000685090.1:n.3655T>A
ENST00000685232.1:n.1946T>A
ENST00000688574.1:n.1833T>A
ENST00000691124.1:n.4686T>A
ENST00000342988.8:c.*66T>A MANE Select ENSP00000341551.3:n.*66T>A
ENST00000342988.7:c.*66T>A ENSP00000341551.3:n.*66T>A
ENST00000398417.6:c.*66T>A ENSP00000381452.1:n.*66T>A
ENST00000586253.1:n.447T>A
ENST00000591126.5:n.3726T>A
ENST00000611848.1:c.1038T>A
NM_005359.5:c.*66T>A , LRG_318t1:c.*66T>A NP_005350.1:n.*66T>A
NM_005359.6:c.*66T>A MANE Select NP_005350.1:n.*66T>A