Canonical Allele Identifier: CA2302981539
Gene: SMAD4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.51067126G= , CM000680.2:g.51067126G= GRCh38
NC_000018.9:g.48593496G= , CM000680.1:g.48593496G= GRCh37
NC_000018.8:g.46847494G= NCBI36
NG_013013.2:g.104087G= , LRG_318:g.104087G=

Transcript Alleles

HGVS Amino-acid change
ENST00000588860.6:c.1247G= ENSP00000465878.2:p.Arg416=
ENST00000589076.6:c.1247G= ENSP00000466934.2:p.Arg416=
ENST00000589941.2:c.1247G= ENSP00000465874.2:p.Arg416=
ENST00000590061.2:c.1247G= ENSP00000464772.2:p.Arg416=
ENST00000593223.2:c.1247G= ENSP00000466118.2:p.Arg416=
ENST00000611848.2:c.1247G= ENSP00000478613.2:p.Arg416=
ENST00000684953.1:n.2619G=
ENST00000685090.1:n.1698G=
ENST00000685232.1:n.1355G=
ENST00000688574.1:n.1355G=
ENST00000691124.1:n.2729G=
ENST00000342988.8:c.1247G= MANE Select ENSP00000341551.3:p.Arg416=
ENST00000342988.7:c.1247G= ENSP00000341551.3:p.Arg416=
ENST00000398417.6:c.1247G= ENSP00000381452.1:p.Arg416=
ENST00000588745.5:c.959G= ENSP00000464901.1:p.Arg320=
ENST00000590499.1:n.305G=
ENST00000591126.5:n.3248G=
ENST00000592186.5:c.955+7210G= ENSP00000468611.1:n.955+7210G=
ENST00000593223.1:c.14G= ENSP00000466118.1:p.Arg5=
ENST00000611848.1:c.447G=
NM_005359.5:c.1247G= , LRG_318t1:c.1247G= NP_005350.1:p.Arg416=
NM_005359.6:c.1247G= MANE Select NP_005350.1:p.Arg416=