Canonical Allele Identifier: CA187376

Gene: SMAD4

Linked Data

• ClinVar Variation Id: 183978
• ClinVar RCV Id: RCV000163070
• dbSNP Id: rs786201200
• MyVariant Identifiers: chr18:g.48593491dupA (hg19) ; chr18:g.51067121dupA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51067121dup , CM000680.2:g.51067121dup	GRCh38
NC_000018.9:g.48593491dup , CM000680.1:g.48593491dup	GRCh37
NC_000018.8:g.46847489dup	NCBI36
NG_013013.2:g.104082dup , LRG_318:g.104082dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588860.6:c.1242dup	ENSP00000465878.2:p.Asp415ArgfsTer14
ENST00000589076.6:c.1242dup	ENSP00000466934.2:p.Asp415ArgfsTer14
ENST00000589941.2:c.1242dup	ENSP00000465874.2:p.Asp415ArgfsTer14
ENST00000590061.2:c.1242dup	ENSP00000464772.2:p.Asp415ArgfsTer14
ENST00000593223.2:c.1242dup	ENSP00000466118.2:p.Asp415ArgfsTer14
ENST00000611848.2:c.1242dup	ENSP00000478613.2:p.Asp415ArgfsTer14
ENST00000684953.1:n.2614dup
ENST00000685090.1:n.1693dup
ENST00000685232.1:n.1350dup
ENST00000688574.1:n.1350dup
ENST00000691124.1:n.2724dup
ENST00000342988.8:c.1242dup MANE Select	ENSP00000341551.3:p.Asp415ArgfsTer14
ENST00000342988.7:c.1242dup	ENSP00000341551.3:p.Asp415ArgfsTer14
ENST00000398417.6:c.1242dup	ENSP00000381452.1:p.Asp415ArgfsTer14
ENST00000588745.5:c.954dup	ENSP00000464901.1:p.Asp319ArgfsTer14
ENST00000590499.1:n.300dup
ENST00000591126.5:n.3243dup
ENST00000592186.5:c.955+7205dup	ENSP00000468611.1:n.955+7205dup
ENST00000593223.1:c.9dup	ENSP00000466118.1:p.Asp4ArgfsTer14
ENST00000611848.1:c.442dup
NM_005359.5:c.1242dup , LRG_318t1:c.1242dup	NP_005350.1:p.Asp415ArgfsTer14
NM_005359.6:c.1242dup MANE Select	NP_005350.1:p.Asp415ArgfsTer14