Canonical Allele Identifier: CA402464720

Gene: SMAD4

Linked Data

• gnomAD v4: 18-51067024-A-G
• COSMIC: COSM6191626
• MyVariant Identifiers: chr18:g.48593394A>G (hg19) ; chr18:g.51067024A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51067024A>G , CM000680.2:g.51067024A>G	GRCh38
NC_000018.9:g.48593394A>G , CM000680.1:g.48593394A>G	GRCh37
NC_000018.8:g.46847392A>G	NCBI36
NG_013013.2:g.103985A>G , LRG_318:g.103985A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000588860.6:c.1145A>G	ENSP00000465878.2:p.His382Arg
ENST00000589076.6:c.1145A>G	ENSP00000466934.2:p.His382Arg
ENST00000589941.2:c.1145A>G	ENSP00000465874.2:p.His382Arg
ENST00000590061.2:c.1145A>G	ENSP00000464772.2:p.His382Arg
ENST00000593223.2:c.1145A>G	ENSP00000466118.2:p.His382Arg
ENST00000611848.2:c.1145A>G	ENSP00000478613.2:p.His382Arg
ENST00000684953.1:n.2517A>G
ENST00000685090.1:n.1596A>G
ENST00000685232.1:n.1253A>G
ENST00000688574.1:n.1253A>G
ENST00000691124.1:n.2627A>G
ENST00000342988.8:c.1145A>G MANE Select	ENSP00000341551.3:p.His382Arg
ENST00000342988.7:c.1145A>G	ENSP00000341551.3:p.His382Arg
ENST00000398417.6:c.1145A>G	ENSP00000381452.1:p.His382Arg
ENST00000588745.5:c.857A>G	ENSP00000464901.1:p.His286Arg
ENST00000590499.1:n.203A>G
ENST00000591126.5:n.3146A>G
ENST00000592186.5:c.955+7108A>G	ENSP00000468611.1:n.955+7108A>G
ENST00000611848.1:c.345A>G
NM_005359.5:c.1145A>G , LRG_318t1:c.1145A>G	NP_005350.1:p.His382Arg
NM_005359.6:c.1145A>G MANE Select	NP_005350.1:p.His382Arg