Canonical Allele Identifier: CA8966025

Gene: SMAD4

Linked Data

• dbSNP Id: rs145097078
• ExAC: 18:48593467 G / C
• gnomAD v3: 18-51067097-G-C
• gnomAD v4: 18-51067097-G-C
• MyVariant Identifiers: chr18:g.48593467G>C (hg19) ; chr18:g.51067097G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51067097G>C , CM000680.2:g.51067097G>C	GRCh38
NC_000018.9:g.48593467G>C , CM000680.1:g.48593467G>C	GRCh37
NC_000018.8:g.46847465G>C	NCBI36
NG_013013.2:g.104058G>C , LRG_318:g.104058G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000588860.6:c.1218G>C	ENSP00000465878.2:p.Ala406=
ENST00000589076.6:c.1218G>C	ENSP00000466934.2:p.Ala406=
ENST00000589941.2:c.1218G>C	ENSP00000465874.2:p.Ala406=
ENST00000590061.2:c.1218G>C	ENSP00000464772.2:p.Ala406=
ENST00000593223.2:c.1218G>C	ENSP00000466118.2:p.Ala406=
ENST00000611848.2:c.1218G>C	ENSP00000478613.2:p.Ala406=
ENST00000684953.1:n.2590G>C
ENST00000685090.1:n.1669G>C
ENST00000685232.1:n.1326G>C
ENST00000688574.1:n.1326G>C
ENST00000691124.1:n.2700G>C
ENST00000342988.8:c.1218G>C MANE Select	ENSP00000341551.3:p.Ala406=
ENST00000342988.7:c.1218G>C	ENSP00000341551.3:p.Ala406=
ENST00000398417.6:c.1218G>C	ENSP00000381452.1:p.Ala406=
ENST00000588745.5:c.930G>C	ENSP00000464901.1:p.Ala310=
ENST00000590499.1:n.276G>C
ENST00000591126.5:n.3219G>C
ENST00000592186.5:c.955+7181G>C	ENSP00000468611.1:n.955+7181G>C
ENST00000611848.1:c.418G>C
NM_005359.5:c.1218G>C , LRG_318t1:c.1218G>C	NP_005350.1:p.Ala406=
NM_005359.6:c.1218G>C MANE Select	NP_005350.1:p.Ala406=