Canonical Allele Identifier: CA503873996

Gene: SMAD4

Linked Data

• ClinVar Variation Id: 2024029
• ClinVar RCV Id: RCV002875999
• dbSNP Id: rs1158531603
• gnomAD v2: 18-48604684-G-A
• gnomAD v4: 18-51078314-G-A
• MyVariant Identifiers: chr18:g.48604684G>A (hg19) ; chr18:g.51078314G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51078314G>A , CM000680.2:g.51078314G>A	GRCh38
NC_000018.9:g.48604684G>A , CM000680.1:g.48604684G>A	GRCh37
NC_000018.8:g.46858682G>A	NCBI36
NG_013013.2:g.115275G>A , LRG_318:g.115275G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000588860.6:c.1506G>A	ENSP00000465878.2:p.Arg502=
ENST00000589076.6:c.1506G>A	ENSP00000466934.2:p.Arg502=
ENST00000589941.2:c.1506G>A	ENSP00000465874.2:p.Arg502=
ENST00000590061.2:c.1506G>A	ENSP00000464772.2:p.Arg502=
ENST00000593223.2:c.*1503G>A	ENSP00000466118.2:n.*1503G>A
ENST00000611848.2:c.*158G>A	ENSP00000478613.2:n.*158G>A
ENST00000684953.1:n.3521G>A
ENST00000685090.1:n.3436G>A
ENST00000685232.1:n.1727G>A
ENST00000688574.1:n.1614G>A
ENST00000691124.1:n.4467G>A
ENST00000342988.8:c.1506G>A MANE Select	ENSP00000341551.3:p.Arg502=
ENST00000342988.7:c.1506G>A	ENSP00000341551.3:p.Arg502=
ENST00000398417.6:c.1506G>A	ENSP00000381452.1:p.Arg502=
ENST00000586253.1:n.228G>A
ENST00000588745.5:c.1218G>A	ENSP00000464901.1:p.Arg406=
ENST00000591126.5:n.3507G>A
ENST00000592186.5:c.1153G>A	ENSP00000468611.1:n.1153G>A
ENST00000611848.1:c.819G>A
NM_005359.5:c.1506G>A , LRG_318t1:c.1506G>A	NP_005350.1:p.Arg502=
NM_005359.6:c.1506G>A MANE Select	NP_005350.1:p.Arg502=