Canonical Allele Identifier: CA503873291

Gene: SMAD4

Linked Data

• MyVariant Identifiers: chr18:g.48573375A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51047005A>G , CM000680.2:g.51047005A>G	GRCh38
NC_000018.9:g.48573375A>G , CM000680.1:g.48573375A>G	GRCh37
NC_000018.8:g.46827373A>G	NCBI36
NG_013013.2:g.83966A>G , LRG_318:g.83966A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588860.6:c.-42A>G	ENSP00000465878.2:n.-42A>G
ENST00000589076.6:c.-42A>G	ENSP00000466934.2:n.-42A>G
ENST00000589941.2:c.-42A>G	ENSP00000465874.2:n.-42A>G
ENST00000590061.2:c.-42A>G	ENSP00000464772.2:n.-42A>G
ENST00000593223.2:c.-42A>G	ENSP00000466118.2:n.-42A>G
ENST00000611848.2:c.-42A>G	ENSP00000478613.2:n.-42A>G
ENST00000342988.8:c.-42A>G MANE Select	ENSP00000341551.3:n.-42A>G
ENST00000342988.7:c.-42A>G	ENSP00000341551.3:n.-42A>G
ENST00000398417.6:c.-42A>G	ENSP00000381452.1:n.-42A>G
ENST00000588256.1:n.420A>G
ENST00000588860.5:c.-42A>G	ENSP00000465878.1:n.-42A>G
ENST00000589076.5:c.-42A>G	ENSP00000466934.1:n.-42A>G
ENST00000589941.1:c.-42A>G	ENSP00000465874.1:n.-42A>G
ENST00000590061.1:c.-42A>G	ENSP00000464772.1:n.-42A>G
ENST00000590722.2:c.243A>G	ENSP00000465737.1:p.Arg81=
ENST00000591914.5:c.-42A>G	ENSP00000466941.1:n.-42A>G
ENST00000592911.5:n.28-1681A>G
NM_005359.5:c.-42A>G , LRG_318t1:c.-42A>G	NP_005350.1:n.-42A>G
NM_005359.6:c.-42A>G MANE Select	NP_005350.1:n.-42A>G