Canonical Allele Identifier: CA2302986886
Gene: SMAD4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.51078313G= , CM000680.2:g.51078313G= GRCh38
NC_000018.9:g.48604683G= , CM000680.1:g.48604683G= GRCh37
NC_000018.8:g.46858681G= NCBI36
NG_013013.2:g.115274G= , LRG_318:g.115274G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000588860.6:c.1505G= ENSP00000465878.2:p.Arg502=
ENST00000589076.6:c.1505G= ENSP00000466934.2:p.Arg502=
ENST00000589941.2:c.1505G= ENSP00000465874.2:p.Arg502=
ENST00000590061.2:c.1505G= ENSP00000464772.2:p.Arg502=
ENST00000593223.2:c.*1502G= ENSP00000466118.2:n.*1502G=
ENST00000611848.2:c.*157G= ENSP00000478613.2:n.*157G=
ENST00000684953.1:n.3520G=
ENST00000685090.1:n.3435G=
ENST00000685232.1:n.1726G=
ENST00000688574.1:n.1613G=
ENST00000691124.1:n.4466G=
ENST00000342988.8:c.1505G= MANE Select ENSP00000341551.3:p.Arg502=
ENST00000342988.7:c.1505G= ENSP00000341551.3:p.Arg502=
ENST00000398417.6:c.1505G= ENSP00000381452.1:p.Arg502=
ENST00000586253.1:n.227G=
ENST00000588745.5:c.1217G= ENSP00000464901.1:p.Arg406=
ENST00000591126.5:n.3506G=
ENST00000592186.5:c.1152G= ENSP00000468611.1:n.1152G=
ENST00000611848.1:c.818G=
NM_005359.5:c.1505G= , LRG_318t1:c.1505G= NP_005350.1:p.Arg502=
NM_005359.6:c.1505G= MANE Select NP_005350.1:p.Arg502=