Canonical Allele Identifier: CA503874245

Gene: SMAD4

Linked Data

• ClinVar Variation Id: 1568223
• ClinVar RCV Id: RCV002216882
• dbSNP Id: rs2144452307
• MyVariant Identifiers: chr18:g.48593470C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51067100C>G , CM000680.2:g.51067100C>G	GRCh38
NC_000018.9:g.48593470C>G , CM000680.1:g.48593470C>G	GRCh37
NC_000018.8:g.46847468C>G	NCBI36
NG_013013.2:g.104061C>G , LRG_318:g.104061C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588860.6:c.1221C>G	ENSP00000465878.2:p.Val407=
ENST00000589076.6:c.1221C>G	ENSP00000466934.2:p.Val407=
ENST00000589941.2:c.1221C>G	ENSP00000465874.2:p.Val407=
ENST00000590061.2:c.1221C>G	ENSP00000464772.2:p.Val407=
ENST00000593223.2:c.1221C>G	ENSP00000466118.2:p.Val407=
ENST00000611848.2:c.1221C>G	ENSP00000478613.2:p.Val407=
ENST00000684953.1:n.2593C>G
ENST00000685090.1:n.1672C>G
ENST00000685232.1:n.1329C>G
ENST00000688574.1:n.1329C>G
ENST00000691124.1:n.2703C>G
ENST00000342988.8:c.1221C>G MANE Select	ENSP00000341551.3:p.Val407=
ENST00000342988.7:c.1221C>G	ENSP00000341551.3:p.Val407=
ENST00000398417.6:c.1221C>G	ENSP00000381452.1:p.Val407=
ENST00000588745.5:c.933C>G	ENSP00000464901.1:p.Val311=
ENST00000590499.1:n.279C>G
ENST00000591126.5:n.3222C>G
ENST00000592186.5:c.955+7184C>G	ENSP00000468611.1:n.955+7184C>G
ENST00000611848.1:c.421C>G
NM_005359.5:c.1221C>G , LRG_318t1:c.1221C>G	NP_005350.1:p.Val407=
NM_005359.6:c.1221C>G MANE Select	NP_005350.1:p.Val407=