Canonical Allele Identifier: CA2572552892

Gene: SMAD4

Linked Data

• dbSNP Id: rs1910529705
• gnomAD v4: 18-51078494-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51078494C>A , CM000680.2:g.51078494C>A	GRCh38
NC_000018.9:g.48604864C>A , CM000680.1:g.48604864C>A	GRCh37
NC_000018.8:g.46858862C>A	NCBI36
NG_013013.2:g.115455C>A , LRG_318:g.115455C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588860.6:c.*27C>A	ENSP00000465878.2:n.*27C>A
ENST00000589076.6:c.*27C>A	ENSP00000466934.2:n.*27C>A
ENST00000589941.2:c.*27C>A	ENSP00000465874.2:n.*27C>A
ENST00000590061.2:c.*27C>A	ENSP00000464772.2:n.*27C>A
ENST00000593223.2:c.*1683C>A	ENSP00000466118.2:n.*1683C>A
ENST00000611848.2:c.*338C>A	ENSP00000478613.2:n.*338C>A
ENST00000684953.1:n.3701C>A
ENST00000685090.1:n.3616C>A
ENST00000685232.1:n.1907C>A
ENST00000688574.1:n.1794C>A
ENST00000691124.1:n.4647C>A
ENST00000342988.8:c.*27C>A MANE Select	ENSP00000341551.3:n.*27C>A
ENST00000342988.7:c.*27C>A	ENSP00000341551.3:n.*27C>A
ENST00000398417.6:c.*27C>A	ENSP00000381452.1:n.*27C>A
ENST00000586253.1:n.408C>A
ENST00000591126.5:n.3687C>A
ENST00000611848.1:c.999C>A
NM_005359.5:c.*27C>A , LRG_318t1:c.*27C>A	NP_005350.1:n.*27C>A
NM_005359.6:c.*27C>A MANE Select	NP_005350.1:n.*27C>A