Canonical Allele Identifier: CA402463698

Gene: SMAD4

Linked Data

• ClinVar Variation Id: 2574387
• ClinVar RCV Id: RCV003318969
• MyVariant Identifiers: chr18:g.48586265C>A (hg19) ; chr18:g.51059895C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51059895C>A , CM000680.2:g.51059895C>A	GRCh38
NC_000018.9:g.48586265C>A , CM000680.1:g.48586265C>A	GRCh37
NC_000018.8:g.46840263C>A	NCBI36
NG_013013.2:g.96856C>A , LRG_318:g.96856C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588860.6:c.934C>A	ENSP00000465878.2:p.Pro312Thr
ENST00000589076.6:c.934C>A	ENSP00000466934.2:p.Pro312Thr
ENST00000589941.2:c.934C>A	ENSP00000465874.2:p.Pro312Thr
ENST00000590061.2:c.934C>A	ENSP00000464772.2:p.Pro312Thr
ENST00000593223.2:c.934C>A	ENSP00000466118.2:p.Pro312Thr
ENST00000611848.2:c.934C>A	ENSP00000478613.2:p.Pro312Thr
ENST00000684953.1:n.2306C>A
ENST00000685090.1:n.1385C>A
ENST00000685232.1:n.1042C>A
ENST00000688307.1:n.185C>A
ENST00000688574.1:n.1042C>A
ENST00000688903.1:n.1148C>A
ENST00000690892.1:n.1042C>A
ENST00000342988.8:c.934C>A MANE Select	ENSP00000341551.3:p.Pro312Thr
ENST00000342988.7:c.934C>A	ENSP00000341551.3:p.Pro312Thr
ENST00000398417.6:c.934C>A	ENSP00000381452.1:p.Pro312Thr
ENST00000588745.5:c.667+4902C>A	ENSP00000464901.1:n.667+4902C>A
ENST00000591126.5:n.2935C>A
ENST00000592186.5:c.934C>A	ENSP00000468611.1:p.Pro312Thr
ENST00000611848.1:c.134C>A
NM_005359.5:c.934C>A , LRG_318t1:c.934C>A	NP_005350.1:p.Pro312Thr
NM_005359.6:c.934C>A MANE Select	NP_005350.1:p.Pro312Thr