Canonical Allele Identifier: CA402464188

Gene: SMAD4

Linked Data

• ClinVar Variation Id: 1779536
• ClinVar RCV Id: RCV002407588
• MyVariant Identifiers: chr18:g.48591841T>G (hg19) ; chr18:g.51065471T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51065471T>G , CM000680.2:g.51065471T>G	GRCh38
NC_000018.9:g.48591841T>G , CM000680.1:g.48591841T>G	GRCh37
NC_000018.8:g.46845839T>G	NCBI36
NG_013013.2:g.102432T>G , LRG_318:g.102432T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588860.6:c.1004T>G	ENSP00000465878.2:p.Val335Gly
ENST00000589076.6:c.1004T>G	ENSP00000466934.2:p.Val335Gly
ENST00000589941.2:c.1004T>G	ENSP00000465874.2:p.Val335Gly
ENST00000590061.2:c.1004T>G	ENSP00000464772.2:p.Val335Gly
ENST00000593223.2:c.1004T>G	ENSP00000466118.2:p.Val335Gly
ENST00000611848.2:c.1004T>G	ENSP00000478613.2:p.Val335Gly
ENST00000684953.1:n.2376T>G
ENST00000685090.1:n.1455T>G
ENST00000685232.1:n.1112T>G
ENST00000688307.1:n.255T>G
ENST00000688574.1:n.1112T>G
ENST00000688903.1:n.1218T>G
ENST00000691124.1:n.2486T>G
ENST00000342988.8:c.1004T>G MANE Select	ENSP00000341551.3:p.Val335Gly
ENST00000342988.7:c.1004T>G	ENSP00000341551.3:p.Val335Gly
ENST00000398417.6:c.1004T>G	ENSP00000381452.1:p.Val335Gly
ENST00000588745.5:c.716T>G	ENSP00000464901.1:p.Val239Gly
ENST00000591126.5:n.3005T>G
ENST00000592186.5:c.955+5555T>G	ENSP00000468611.1:n.955+5555T>G
ENST00000611848.1:c.204T>G
NM_005359.5:c.1004T>G , LRG_318t1:c.1004T>G	NP_005350.1:p.Val335Gly
NM_005359.6:c.1004T>G MANE Select	NP_005350.1:p.Val335Gly