Canonical Allele Identifier: CA402458791

Gene: SMAD4

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51048839C>G , CM000680.2:g.51048839C>G	GRCh38
NC_000018.9:g.48575209C>G , CM000680.1:g.48575209C>G	GRCh37
NC_000018.8:g.46829207C>G	NCBI36
NG_013013.2:g.85800C>G , LRG_318:g.85800C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_005359.6:c.403C>G MANE Select	NP_005350.1:p.Arg135Gly
ENST00000342988.8:c.403C>G MANE Select	ENSP00000341551.3:p.Arg135Gly
NM_005359.5:c.403C>G , LRG_318t1:c.403C>G	NP_005350.1:p.Arg135Gly
ENST00000342988.7:c.403C>G	ENSP00000341551.3:p.Arg135Gly
ENST00000398417.6:c.403C>G	ENSP00000381452.1:p.Arg135Gly
ENST00000588745.5:c.403C>G	ENSP00000464901.1:p.Arg135Gly
ENST00000588860.6:c.403C>G	ENSP00000465878.2:p.Arg135Gly
ENST00000589076.6:c.403C>G	ENSP00000466934.2:p.Arg135Gly
ENST00000589706.1:n.271C>G
ENST00000589941.2:c.403C>G	ENSP00000465874.2:p.Arg135Gly
ENST00000590061.1:c.403C>G	ENSP00000464772.1:p.Arg135Gly
ENST00000590061.2:c.403C>G	ENSP00000464772.2:p.Arg135Gly
ENST00000590722.2:c.*426C>G	ENSP00000465737.1:n.*426C>G
ENST00000591914.5:c.403C>G	ENSP00000466941.1:p.Arg135Gly
ENST00000592186.5:c.403C>G	ENSP00000468611.1:p.Arg135Gly
ENST00000592911.5:n.181C>G
ENST00000593223.2:c.403C>G	ENSP00000466118.2:p.Arg135Gly
ENST00000611848.2:c.403C>G	ENSP00000478613.2:p.Arg135Gly