Canonical Allele Identifier: CA2735213721

Gene: SMAD4

Linked Data

• dbSNP Id: rs2144407144

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51049206G>A , CM000680.2:g.51049206G>A	GRCh38
NC_000018.9:g.48575576G>A , CM000680.1:g.48575576G>A	GRCh37
NC_000018.8:g.46829574G>A	NCBI36
NG_013013.2:g.86167G>A , LRG_318:g.86167G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000588860.6:c.425-89G>A	ENSP00000465878.2:n.425-89G>A
ENST00000589076.6:c.425-89G>A	ENSP00000466934.2:n.425-89G>A
ENST00000589941.2:c.425-89G>A	ENSP00000465874.2:n.425-89G>A
ENST00000590061.2:c.425-89G>A	ENSP00000464772.2:n.425-89G>A
ENST00000593223.2:c.425-89G>A	ENSP00000466118.2:n.425-89G>A
ENST00000611848.2:c.425-89G>A	ENSP00000478613.2:n.425-89G>A
ENST00000342988.8:c.425-89G>A MANE Select	ENSP00000341551.3:n.425-89G>A
ENST00000342988.7:c.425-89G>A	ENSP00000341551.3:n.425-89G>A
ENST00000398417.6:c.425-89G>A	ENSP00000381452.1:n.425-89G>A
ENST00000588745.5:c.425-89G>A	ENSP00000464901.1:n.425-89G>A
ENST00000589706.1:n.293-89G>A
ENST00000590722.2:c.*448-89G>A	ENSP00000465737.1:n.*448-89G>A
ENST00000591914.5:c.425-89G>A	ENSP00000466941.1:n.425-89G>A
ENST00000592186.5:c.425-89G>A	ENSP00000468611.1:n.425-89G>A
ENST00000592911.5:n.203-89G>A
NM_005359.5:c.425-89G>A , LRG_318t1:c.425-89G>A	NP_005350.1:n.425-89G>A
NM_005359.6:c.425-89G>A MANE Select	NP_005350.1:n.425-89G>A