Canonical Allele Identifier: CA2735220267

Gene: SMAD4

Linked Data

• dbSNP Id: rs2144446163

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51065407C>G , CM000680.2:g.51065407C>G	GRCh38
NC_000018.9:g.48591777C>G , CM000680.1:g.48591777C>G	GRCh37
NC_000018.8:g.46845775C>G	NCBI36
NG_013013.2:g.102368C>G , LRG_318:g.102368C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000588860.6:c.956-16C>G	ENSP00000465878.2:n.956-16C>G
ENST00000589076.6:c.956-16C>G	ENSP00000466934.2:n.956-16C>G
ENST00000589941.2:c.956-16C>G	ENSP00000465874.2:n.956-16C>G
ENST00000590061.2:c.956-16C>G	ENSP00000464772.2:n.956-16C>G
ENST00000593223.2:c.956-16C>G	ENSP00000466118.2:n.956-16C>G
ENST00000611848.2:c.956-16C>G	ENSP00000478613.2:n.956-16C>G
ENST00000684953.1:n.2328-16C>G
ENST00000685090.1:n.1407-16C>G
ENST00000685232.1:n.1064-16C>G
ENST00000688307.1:n.207-16C>G
ENST00000688574.1:n.1064-16C>G
ENST00000688903.1:n.1170-16C>G
ENST00000691124.1:n.2422C>G
ENST00000342988.8:c.956-16C>G MANE Select	ENSP00000341551.3:n.956-16C>G
ENST00000342988.7:c.956-16C>G	ENSP00000341551.3:n.956-16C>G
ENST00000398417.6:c.956-16C>G	ENSP00000381452.1:n.956-16C>G
ENST00000588745.5:c.668-16C>G	ENSP00000464901.1:n.668-16C>G
ENST00000591126.5:n.2957-16C>G
ENST00000592186.5:c.955+5491C>G	ENSP00000468611.1:n.955+5491C>G
ENST00000611848.1:c.156-16C>G
NM_005359.5:c.956-16C>G , LRG_318t1:c.956-16C>G	NP_005350.1:n.956-16C>G
NM_005359.6:c.956-16C>G MANE Select	NP_005350.1:n.956-16C>G