Canonical Allele Identifier: CA915951536

Gene: SMAD4

Linked Data

• ClinVar Variation Id: 801279
• ClinVar RCV Id: RCV002400160
• dbSNP Id: rs1599195433

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51065512dup , CM000680.2:g.51065512dup	GRCh38
NC_000018.9:g.48591882dup , CM000680.1:g.48591882dup	GRCh37
NC_000018.8:g.46845880dup	NCBI36
NG_013013.2:g.102473dup , LRG_318:g.102473dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000588860.6:c.1045dup	ENSP00000465878.2:p.Thr349AsnfsTer3
ENST00000589076.6:c.1045dup	ENSP00000466934.2:p.Thr349AsnfsTer3
ENST00000589941.2:c.1045dup	ENSP00000465874.2:p.Thr349AsnfsTer3
ENST00000590061.2:c.1045dup	ENSP00000464772.2:p.Thr349AsnfsTer3
ENST00000593223.2:c.1045dup	ENSP00000466118.2:p.Thr349AsnfsTer3
ENST00000611848.2:c.1045dup	ENSP00000478613.2:p.Thr349AsnfsTer3
ENST00000684953.1:n.2417dup
ENST00000685090.1:n.1496dup
ENST00000685232.1:n.1153dup
ENST00000688307.1:n.296dup
ENST00000688574.1:n.1153dup
ENST00000688903.1:n.1259dup
ENST00000691124.1:n.2527dup
ENST00000342988.8:c.1045dup MANE Select	ENSP00000341551.3:p.Thr349AsnfsTer3
ENST00000342988.7:c.1045dup	ENSP00000341551.3:p.Thr349AsnfsTer3
ENST00000398417.6:c.1045dup	ENSP00000381452.1:p.Thr349AsnfsTer3
ENST00000588745.5:c.757dup	ENSP00000464901.1:p.Thr253AsnfsTer3
ENST00000591126.5:n.3046dup
ENST00000592186.5:c.955+5596dup	ENSP00000468611.1:n.955+5596dup
ENST00000611848.1:c.245dup
NM_005359.5:c.1045dup , LRG_318t1:c.1045dup	NP_005350.1:p.Thr349AsnfsTer3
NM_005359.6:c.1045dup MANE Select	NP_005350.1:p.Thr349AsnfsTer3