Canonical Allele Identifier: CA2302981516
Gene: SMAD4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.51067094C= , CM000680.2:g.51067094C= GRCh38
NC_000018.9:g.48593464C= , CM000680.1:g.48593464C= GRCh37
NC_000018.8:g.46847462C= NCBI36
NG_013013.2:g.104055C= , LRG_318:g.104055C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000588860.6:c.1215C= ENSP00000465878.2:p.His405=
ENST00000589076.6:c.1215C= ENSP00000466934.2:p.His405=
ENST00000589941.2:c.1215C= ENSP00000465874.2:p.His405=
ENST00000590061.2:c.1215C= ENSP00000464772.2:p.His405=
ENST00000593223.2:c.1215C= ENSP00000466118.2:p.His405=
ENST00000611848.2:c.1215C= ENSP00000478613.2:p.His405=
ENST00000684953.1:n.2587C=
ENST00000685090.1:n.1666C=
ENST00000685232.1:n.1323C=
ENST00000688574.1:n.1323C=
ENST00000691124.1:n.2697C=
ENST00000342988.8:c.1215C= MANE Select ENSP00000341551.3:p.His405=
ENST00000342988.7:c.1215C= ENSP00000341551.3:p.His405=
ENST00000398417.6:c.1215C= ENSP00000381452.1:p.His405=
ENST00000588745.5:c.927C= ENSP00000464901.1:p.His309=
ENST00000590499.1:n.273C=
ENST00000591126.5:n.3216C=
ENST00000592186.5:c.955+7178C= ENSP00000468611.1:n.955+7178C=
ENST00000611848.1:c.415C=
NM_005359.5:c.1215C= , LRG_318t1:c.1215C= NP_005350.1:p.His405=
NM_005359.6:c.1215C= MANE Select NP_005350.1:p.His405=