Canonical Allele Identifier: CA2573155420

Gene: SMAD4

Linked Data

• ClinVar Variation Id: 1457361
• ClinVar RCV Id: RCV001953721
• dbSNP Id: rs2144429483

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.51058454dup , CM000680.2:g.51058454dup	GRCh38
NC_000018.9:g.48584824dup , CM000680.1:g.48584824dup	GRCh37
NC_000018.8:g.46838822dup	NCBI36
NG_013013.2:g.95415dup , LRG_318:g.95415dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000588860.6:c.902dup	ENSP00000465878.2:p.Tyr301Ter
ENST00000589076.6:c.902dup	ENSP00000466934.2:p.Tyr301Ter
ENST00000589941.2:c.902dup	ENSP00000465874.2:p.Tyr301Ter
ENST00000590061.2:c.902dup	ENSP00000464772.2:p.Tyr301Ter
ENST00000593223.2:c.902dup	ENSP00000466118.2:p.Tyr301Ter
ENST00000611848.2:c.902dup	ENSP00000478613.2:p.Tyr301Ter
ENST00000684953.1:n.2274dup
ENST00000685232.1:n.1010dup
ENST00000688307.1:n.156-1412dup
ENST00000688574.1:n.1010dup
ENST00000688903.1:n.1116dup
ENST00000690892.1:n.1010dup
ENST00000342988.8:c.902dup MANE Select	ENSP00000341551.3:p.Tyr301Ter
ENST00000342988.7:c.902dup	ENSP00000341551.3:p.Tyr301Ter
ENST00000398417.6:c.902dup	ENSP00000381452.1:p.Tyr301Ter
ENST00000588745.5:c.667+3461dup	ENSP00000464901.1:n.667+3461dup
ENST00000591126.5:n.2903dup
ENST00000592186.5:c.902dup	ENSP00000468611.1:p.Tyr301Ter
ENST00000611848.1:c.102dup
NM_005359.5:c.902dup , LRG_318t1:c.902dup	NP_005350.1:p.Tyr301Ter
NM_005359.6:c.902dup MANE Select	NP_005350.1:p.Tyr301Ter