Canonical Allele Identifier: CA2735215789

Gene: SMAD4

Linked Data

• dbSNP Id: rs2144480134

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51078495T>A , CM000680.2:g.51078495T>A	GRCh38
NC_000018.9:g.48604865T>A , CM000680.1:g.48604865T>A	GRCh37
NC_000018.8:g.46858863T>A	NCBI36
NG_013013.2:g.115456T>A , LRG_318:g.115456T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588860.6:c.*28T>A	ENSP00000465878.2:n.*28T>A
ENST00000589076.6:c.*28T>A	ENSP00000466934.2:n.*28T>A
ENST00000589941.2:c.*28T>A	ENSP00000465874.2:n.*28T>A
ENST00000590061.2:c.*28T>A	ENSP00000464772.2:n.*28T>A
ENST00000593223.2:c.*1684T>A	ENSP00000466118.2:n.*1684T>A
ENST00000611848.2:c.*339T>A	ENSP00000478613.2:n.*339T>A
ENST00000684953.1:n.3702T>A
ENST00000685090.1:n.3617T>A
ENST00000685232.1:n.1908T>A
ENST00000688574.1:n.1795T>A
ENST00000691124.1:n.4648T>A
ENST00000342988.8:c.*28T>A MANE Select	ENSP00000341551.3:n.*28T>A
ENST00000342988.7:c.*28T>A	ENSP00000341551.3:n.*28T>A
ENST00000398417.6:c.*28T>A	ENSP00000381452.1:n.*28T>A
ENST00000586253.1:n.409T>A
ENST00000591126.5:n.3688T>A
ENST00000611848.1:c.1000T>A
NM_005359.5:c.*28T>A , LRG_318t1:c.*28T>A	NP_005350.1:n.*28T>A
NM_005359.6:c.*28T>A MANE Select	NP_005350.1:n.*28T>A