Canonical Allele Identifier: CA2735032576

Gene: SMAD4

Linked Data

• dbSNP Id: rs1039813805

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51078480T>A , CM000680.2:g.51078480T>A	GRCh38
NC_000018.9:g.48604850T>A , CM000680.1:g.48604850T>A	GRCh37
NC_000018.8:g.46858848T>A	NCBI36
NG_013013.2:g.115441T>A , LRG_318:g.115441T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588860.6:c.*13T>A	ENSP00000465878.2:n.*13T>A
ENST00000589076.6:c.*13T>A	ENSP00000466934.2:n.*13T>A
ENST00000589941.2:c.*13T>A	ENSP00000465874.2:n.*13T>A
ENST00000590061.2:c.*13T>A	ENSP00000464772.2:n.*13T>A
ENST00000593223.2:c.*1669T>A	ENSP00000466118.2:n.*1669T>A
ENST00000611848.2:c.*324T>A	ENSP00000478613.2:n.*324T>A
ENST00000684953.1:n.3687T>A
ENST00000685090.1:n.3602T>A
ENST00000685232.1:n.1893T>A
ENST00000688574.1:n.1780T>A
ENST00000691124.1:n.4633T>A
ENST00000342988.8:c.*13T>A MANE Select	ENSP00000341551.3:n.*13T>A
ENST00000342988.7:c.*13T>A	ENSP00000341551.3:n.*13T>A
ENST00000398417.6:c.*13T>A	ENSP00000381452.1:n.*13T>A
ENST00000586253.1:n.394T>A
ENST00000591126.5:n.3673T>A
ENST00000611848.1:c.985T>A
NM_005359.5:c.*13T>A , LRG_318t1:c.*13T>A	NP_005350.1:n.*13T>A
NM_005359.6:c.*13T>A MANE Select	NP_005350.1:n.*13T>A