Canonical Allele Identifier: CA2630855503

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.681818_681820del , CM000678.2:g.681818_681820del GRCh38
NC_000016.9:g.731818_731820del , CM000678.1:g.731818_731820del GRCh37
NC_000016.8:g.671819_671821del NCBI36
NG_034141.1:g.6708_6710del

Transcript Alleles

HGVS Amino-acid Change
ENST00000219548.9:c.550_552del (STUB1) MANE Select ENSP00000219548.4:p.His184del
ENST00000609261.6:c.*976_*978del (JMJD8) MANE Select ENSP00000477481.1:n.*976_*978del
ENST00000219548.8:c.550_552del (STUB1) ENSP00000219548.4:p.His184del
ENST00000412368.6:c.*976_*978del (JMJD8) ENSP00000399475.2:n.*976_*978del
ENST00000563505.5:n.646_648del (STUB1)
ENST00000564316.1:c.149_151del (STUB1)
ENST00000564370.5:c.334_336del (STUB1) ENSP00000456875.1:p.His112del
ENST00000565302.5:n.1855_1857del (JMJD8)
ENST00000565677.5:c.334_336del (STUB1) ENSP00000457228.1:p.His112del
ENST00000566181.2:n.319_321del (STUB1)
ENST00000566408.5:c.267_269del (STUB1)
ENST00000567120.5:n.2058_2060del (JMJD8)
ENST00000567173.5:c.493_495del (STUB1) ENSP00000456591.1:p.His165del
ENST00000568689.5:n.1879_1881del (JMJD8)
ENST00000569248.5:n.1124_1126del (STUB1)
ENST00000609261.5:c.*976_*978del (JMJD8) ENSP00000477481.1:n.*976_*978del
ENST00000620831.4:c.-50+38515_-50+38517del (MSLN) ENSP00000482893.1:n.-50+38515_-50+38517del
NM_001005920.2:c.*976_*978del (JMJD8) NP_001005920.2:n.*976_*978del
NM_001293197.1:c.334_336del (STUB1) NP_001280126.1:p.His112del
NM_005861.3:c.550_552del (STUB1) NP_005852.2:p.His184del
XM_005255295.3:c.*1010_*1012del (JMJD8) XP_005255352.1:n.*1010_*1012del
XM_005255297.3:c.*976_*978del (JMJD8) XP_005255354.1:n.*976_*978del
XM_011522474.1:c.*976_*978del (JMJD8) XP_011520776.1:n.*976_*978del
NM_001005920.3:c.*976_*978del (JMJD8) NP_001005920.3:n.*976_*978del
NM_001323918.2:c.*1010_*1012del (JMJD8) NP_001310847.2:n.*1010_*1012del
NM_001323919.2:c.*976_*978del (JMJD8) NP_001310848.2:n.*976_*978del
NM_001323920.2:c.*976_*978del (JMJD8) NP_001310849.2:n.*976_*978del
NM_001323922.2:c.*1010_*1012del (JMJD8) NP_001310851.2:n.*1010_*1012del
NR_136650.2:n.1869_1871del (JMJD8)
NR_136651.2:n.1874_1876del (JMJD8)
NR_136652.2:n.1784_1786del (JMJD8)
NM_001005920.4:c.*976_*978del (JMJD8) MANE Select NP_001005920.3:n.*976_*978del
NM_005861.4:c.550_552del (STUB1) MANE Select NP_005852.2:p.His184del
NM_001293197.2:c.334_336del (STUB1) NP_001280126.1:p.His112del
NM_001323918.3:c.*1010_*1012del (JMJD8) NP_001310847.2:n.*1010_*1012del
NM_001323919.3:c.*976_*978del (JMJD8) NP_001310848.2:n.*976_*978del
NM_001323920.3:c.*976_*978del (JMJD8) NP_001310849.2:n.*976_*978del
NM_001323922.3:c.*1010_*1012del (JMJD8) NP_001310851.2:n.*1010_*1012del
NR_136650.3:n.1869_1871del (JMJD8)
NR_136651.3:n.1874_1876del (JMJD8)
NR_136652.3:n.1784_1786del (JMJD8)