Canonical Allele Identifier: CA2580095836
Gene: SMAD4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.51058235_51058236dup , CM000680.2:g.51058235_51058236dup GRCh38
NC_000018.9:g.48584605_48584606dup , CM000680.1:g.48584605_48584606dup GRCh37
NC_000018.8:g.46838603_46838604dup NCBI36
NG_013013.2:g.95196_95197dup , LRG_318:g.95196_95197dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000588860.6:c.778_779dup ENSP00000465878.2:p.His261ThrfsTer?
ENST00000589076.6:c.778_779dup ENSP00000466934.2:p.His261ThrfsTer?
ENST00000589941.2:c.778_779dup ENSP00000465874.2:p.His261ThrfsTer?
ENST00000590061.2:c.778_779dup ENSP00000464772.2:p.His261ThrfsTer?
ENST00000593223.2:c.778_779dup ENSP00000466118.2:p.His261ThrfsTer?
ENST00000611848.2:c.778_779dup ENSP00000478613.2:p.His261ThrfsTer?
ENST00000684953.1:n.2150_2151dup
ENST00000685232.1:n.886_887dup
ENST00000688307.1:n.156-1631_156-1630dup
ENST00000688574.1:n.886_887dup
ENST00000688903.1:n.992_993dup
ENST00000690892.1:n.886_887dup
ENST00000342988.8:c.778_779dup MANE Select ENSP00000341551.3:p.His261ThrfsTer?
ENST00000342988.7:c.778_779dup ENSP00000341551.3:p.His261ThrfsTer?
ENST00000398417.6:c.778_779dup ENSP00000381452.1:p.His261ThrfsTer?
ENST00000588745.5:c.667+3242_667+3243dup ENSP00000464901.1:n.667+3242_667+3243dup
ENST00000591126.5:n.2779_2780dup
ENST00000592186.5:c.778_779dup ENSP00000468611.1:p.His261ThrfsTer?
NM_005359.5:c.778_779dup , LRG_318t1:c.778_779dup NP_005350.1:p.His261ThrfsTer?
NM_005359.6:c.778_779dup MANE Select NP_005350.1:p.His261ThrfsTer?