Canonical Allele Identifier: CA780207005

Gene: SMAD4

Linked Data

• dbSNP Id: rs1225071196
• MyVariant Identifiers: chr18:g.48604936T>A (hg19) ; chr18:g.51078566T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51078566T>A , CM000680.2:g.51078566T>A	GRCh38
NC_000018.9:g.48604936T>A , CM000680.1:g.48604936T>A	GRCh37
NC_000018.8:g.46858934T>A	NCBI36
NG_013013.2:g.115527T>A , LRG_318:g.115527T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588860.6:c.*99T>A	ENSP00000465878.2:n.*99T>A
ENST00000589076.6:c.*99T>A	ENSP00000466934.2:n.*99T>A
ENST00000589941.2:c.*99T>A	ENSP00000465874.2:n.*99T>A
ENST00000590061.2:c.*99T>A	ENSP00000464772.2:n.*99T>A
ENST00000593223.2:c.*1755T>A	ENSP00000466118.2:n.*1755T>A
ENST00000611848.2:c.*410T>A	ENSP00000478613.2:n.*410T>A
ENST00000684953.1:n.3773T>A
ENST00000685090.1:n.3688T>A
ENST00000685232.1:n.1979T>A
ENST00000688574.1:n.1866T>A
ENST00000691124.1:n.4719T>A
ENST00000342988.8:c.*99T>A MANE Select	ENSP00000341551.3:n.*99T>A
ENST00000342988.7:c.*99T>A	ENSP00000341551.3:n.*99T>A
ENST00000398417.6:c.*99T>A	ENSP00000381452.1:n.*99T>A
ENST00000586253.1:n.480T>A
ENST00000591126.5:n.3759T>A
ENST00000611848.1:c.1071T>A
NM_005359.5:c.*99T>A , LRG_318t1:c.*99T>A	NP_005350.1:n.*99T>A
NM_005359.6:c.*99T>A MANE Select	NP_005350.1:n.*99T>A