Canonical Allele Identifier: CA402465774

Gene: SMAD4

Linked Data

• dbSNP Id: rs876660045
• MyVariant Identifiers: chr18:g.48604665G>C (hg19) ; chr18:g.51078295G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51078295G>C , CM000680.2:g.51078295G>C	GRCh38
NC_000018.9:g.48604665G>C , CM000680.1:g.48604665G>C	GRCh37
NC_000018.8:g.46858663G>C	NCBI36
NG_013013.2:g.115256G>C , LRG_318:g.115256G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588860.6:c.1487G>C	ENSP00000465878.2:p.Arg496Pro
ENST00000589076.6:c.1487G>C	ENSP00000466934.2:p.Arg496Pro
ENST00000589941.2:c.1487G>C	ENSP00000465874.2:p.Arg496Pro
ENST00000590061.2:c.1487G>C	ENSP00000464772.2:p.Arg496Pro
ENST00000593223.2:c.*1484G>C	ENSP00000466118.2:n.*1484G>C
ENST00000611848.2:c.*139G>C	ENSP00000478613.2:n.*139G>C
ENST00000684953.1:n.3502G>C
ENST00000685090.1:n.3417G>C
ENST00000685232.1:n.1708G>C
ENST00000688574.1:n.1595G>C
ENST00000691124.1:n.4448G>C
ENST00000342988.8:c.1487G>C MANE Select	ENSP00000341551.3:p.Arg496Pro
ENST00000342988.7:c.1487G>C	ENSP00000341551.3:p.Arg496Pro
ENST00000398417.6:c.1487G>C	ENSP00000381452.1:p.Arg496Pro
ENST00000586253.1:n.209G>C
ENST00000588745.5:c.1199G>C	ENSP00000464901.1:p.Arg400Pro
ENST00000591126.5:n.3488G>C
ENST00000592186.5:c.1134G>C	ENSP00000468611.1:n.1134G>C
ENST00000611848.1:c.800G>C
NM_005359.5:c.1487G>C , LRG_318t1:c.1487G>C	NP_005350.1:p.Arg496Pro
NM_005359.6:c.1487G>C MANE Select	NP_005350.1:p.Arg496Pro