Canonical Allele Identifier: CA402464568

Gene: SMAD4

Linked Data

• ClinVar Variation Id: 460525
• ClinVar RCV Id: RCV000533488 ; RCV001185976 ; RCV001770420
• dbSNP Id: rs1555686501
• MyVariant Identifiers: chr18:g.48591963A>G (hg19) ; chr18:g.51065593A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51065593A>G , CM000680.2:g.51065593A>G	GRCh38
NC_000018.9:g.48591963A>G , CM000680.1:g.48591963A>G	GRCh37
NC_000018.8:g.46845961A>G	NCBI36
NG_013013.2:g.102554A>G , LRG_318:g.102554A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588860.6:c.1126A>G	ENSP00000465878.2:p.Ile376Val
ENST00000589076.6:c.1126A>G	ENSP00000466934.2:p.Ile376Val
ENST00000589941.2:c.1126A>G	ENSP00000465874.2:p.Ile376Val
ENST00000590061.2:c.1126A>G	ENSP00000464772.2:p.Ile376Val
ENST00000593223.2:c.1126A>G	ENSP00000466118.2:p.Ile376Val
ENST00000611848.2:c.1126A>G	ENSP00000478613.2:p.Ile376Val
ENST00000684953.1:n.2498A>G
ENST00000685090.1:n.1577A>G
ENST00000685232.1:n.1234A>G
ENST00000688307.1:n.377A>G
ENST00000688574.1:n.1234A>G
ENST00000688903.1:n.1340A>G
ENST00000691124.1:n.2608A>G
ENST00000342988.8:c.1126A>G MANE Select	ENSP00000341551.3:p.Ile376Val
ENST00000342988.7:c.1126A>G	ENSP00000341551.3:p.Ile376Val
ENST00000398417.6:c.1126A>G	ENSP00000381452.1:p.Ile376Val
ENST00000588745.5:c.838A>G	ENSP00000464901.1:p.Ile280Val
ENST00000591126.5:n.3127A>G
ENST00000592186.5:c.955+5677A>G	ENSP00000468611.1:n.955+5677A>G
ENST00000611848.1:c.326A>G
NM_005359.5:c.1126A>G , LRG_318t1:c.1126A>G	NP_005350.1:p.Ile376Val
NM_005359.6:c.1126A>G MANE Select	NP_005350.1:p.Ile376Val