Canonical Allele Identifier: CA2697555502
Gene: SMAD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2769594
ClinVar RCV Id: RCV003597155

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.51047254_51047261del , CM000680.2:g.51047254_51047261del GRCh38
NC_000018.9:g.48573624_48573631del , CM000680.1:g.48573624_48573631del GRCh37
NC_000018.8:g.46827622_46827629del NCBI36
NG_013013.2:g.84215_84222del , LRG_318:g.84215_84222del

Transcript Alleles

HGVS Amino-acid Change
ENST00000588860.6:c.208_215del ENSP00000465878.2:p.Lys70TyrfsTer?
ENST00000589076.6:c.208_215del ENSP00000466934.2:p.Lys70TyrfsTer?
ENST00000589941.2:c.208_215del ENSP00000465874.2:p.Lys70TyrfsTer?
ENST00000590061.2:c.208_215del ENSP00000464772.2:p.Lys70TyrfsTer?
ENST00000593223.2:c.208_215del ENSP00000466118.2:p.Lys70TyrfsTer?
ENST00000611848.2:c.208_215del ENSP00000478613.2:p.Lys70TyrfsTer?
ENST00000342988.8:c.208_215del MANE Select ENSP00000341551.3:p.Lys70TyrfsTer?
ENST00000342988.7:c.208_215del ENSP00000341551.3:p.Lys70TyrfsTer?
ENST00000398417.6:c.208_215del ENSP00000381452.1:p.Lys70TyrfsTer?
ENST00000588745.5:c.208_215del ENSP00000464901.1:p.Lys70TyrfsTer?
ENST00000588860.5:c.208_215del ENSP00000465878.1:p.Lys70TyrfsTer?
ENST00000589076.5:c.208_215del ENSP00000466934.1:p.Lys70TyrfsTer?
ENST00000589706.1:n.76_83del
ENST00000589941.1:c.208_215del ENSP00000465874.1:p.Lys70TyrfsTer?
ENST00000590061.1:c.208_215del ENSP00000464772.1:p.Lys70TyrfsTer?
ENST00000590722.2:c.*231_*238del ENSP00000465737.1:n.*231_*238del
ENST00000591914.5:c.208_215del ENSP00000466941.1:p.Lys70TyrfsTer?
ENST00000592186.5:c.208_215del ENSP00000468611.1:p.Lys70TyrfsTer?
ENST00000592911.5:n.28-1432_28-1425del
NM_005359.5:c.208_215del , LRG_318t1:c.208_215del NP_005350.1:p.Lys70TyrfsTer?
NM_005359.6:c.208_215del MANE Select NP_005350.1:p.Lys70TyrfsTer?