Canonical Allele Identifier: CA402460613

Gene: SMAD4

Linked Data

• ClinVar Variation Id: 2811162
• ClinVar RCV Id: RCV003762437
• dbSNP Id: rs1555685628
• MyVariant Identifiers: chr18:g.48581168G>A (hg19) ; chr18:g.51054798G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51054798G>A , CM000680.2:g.51054798G>A	GRCh38
NC_000018.9:g.48581168G>A , CM000680.1:g.48581168G>A	GRCh37
NC_000018.8:g.46835166G>A	NCBI36
NG_013013.2:g.91759G>A , LRG_318:g.91759G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000588860.6:c.472G>A	ENSP00000465878.2:p.Val158Met
ENST00000589076.6:c.472G>A	ENSP00000466934.2:p.Val158Met
ENST00000589941.2:c.472G>A	ENSP00000465874.2:p.Val158Met
ENST00000590061.2:c.472G>A	ENSP00000464772.2:p.Val158Met
ENST00000593223.2:c.472G>A	ENSP00000466118.2:p.Val158Met
ENST00000611848.2:c.472G>A	ENSP00000478613.2:p.Val158Met
ENST00000684953.1:n.1844G>A
ENST00000342988.8:c.472G>A MANE Select	ENSP00000341551.3:p.Val158Met
ENST00000342988.7:c.472G>A	ENSP00000341551.3:p.Val158Met
ENST00000398417.6:c.472G>A	ENSP00000381452.1:p.Val158Met
ENST00000585448.1:n.341G>A
ENST00000588745.5:c.472G>A	ENSP00000464901.1:p.Val158Met
ENST00000590722.2:c.*648G>A	ENSP00000465737.1:n.*648G>A
ENST00000591126.5:n.2473G>A
ENST00000592186.5:c.472G>A	ENSP00000468611.1:p.Val158Met
ENST00000592911.5:n.250G>A
NM_005359.5:c.472G>A , LRG_318t1:c.472G>A	NP_005350.1:p.Val158Met
NM_005359.6:c.472G>A MANE Select	NP_005350.1:p.Val158Met