Canonical Allele Identifier: CA402462619

Gene: SMAD4

Linked Data

• ClinVar Variation Id: 631311
• ClinVar RCV Id: RCV000777492 ; RCV001221876 ; RCV002360895 ; RCV004001501
• dbSNP Id: rs1443767329
• gnomAD v3: 18-51058136-A-G
• gnomAD v4: 18-51058136-A-G
• MyVariant Identifiers: chr18:g.48584506A>G (hg19) ; chr18:g.51058136A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51058136A>G , CM000680.2:g.51058136A>G	GRCh38
NC_000018.9:g.48584506A>G , CM000680.1:g.48584506A>G	GRCh37
NC_000018.8:g.46838504A>G	NCBI36
NG_013013.2:g.95097A>G , LRG_318:g.95097A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588860.6:c.679A>G	ENSP00000465878.2:p.Ser227Gly
ENST00000589076.6:c.679A>G	ENSP00000466934.2:p.Ser227Gly
ENST00000589941.2:c.679A>G	ENSP00000465874.2:p.Ser227Gly
ENST00000590061.2:c.679A>G	ENSP00000464772.2:p.Ser227Gly
ENST00000593223.2:c.679A>G	ENSP00000466118.2:p.Ser227Gly
ENST00000611848.2:c.679A>G	ENSP00000478613.2:p.Ser227Gly
ENST00000684953.1:n.2051A>G
ENST00000685232.1:n.787A>G
ENST00000688307.1:n.156-1730A>G
ENST00000688574.1:n.787A>G
ENST00000688903.1:n.893A>G
ENST00000690892.1:n.787A>G
ENST00000342988.8:c.679A>G MANE Select	ENSP00000341551.3:p.Ser227Gly
ENST00000342988.7:c.679A>G	ENSP00000341551.3:p.Ser227Gly
ENST00000398417.6:c.679A>G	ENSP00000381452.1:p.Ser227Gly
ENST00000588745.5:c.667+3143A>G	ENSP00000464901.1:n.667+3143A>G
ENST00000590722.2:c.*855A>G	ENSP00000465737.1:n.*855A>G
ENST00000591126.5:n.2680A>G
ENST00000592186.5:c.679A>G	ENSP00000468611.1:p.Ser227Gly
ENST00000592911.5:n.457A>G
NM_005359.5:c.679A>G , LRG_318t1:c.679A>G	NP_005350.1:p.Ser227Gly
NM_005359.6:c.679A>G MANE Select	NP_005350.1:p.Ser227Gly