Canonical Allele Identifier: CA2630855440

Linked Data

gnomAD v4: 16-681807-GC-G

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.681809del , CM000678.2:g.681809del GRCh38
NC_000016.9:g.731809del , CM000678.1:g.731809del GRCh37
NC_000016.8:g.671810del NCBI36
NG_034141.1:g.6699del

Transcript Alleles

HGVS Amino-acid Change
ENST00000219548.9:c.541del (STUB1) MANE Select ENSP00000219548.4:p.Gln181SerfsTer?
ENST00000609261.6:c.*986del (JMJD8) MANE Select ENSP00000477481.1:n.*986del
ENST00000219548.8:c.541del (STUB1) ENSP00000219548.4:p.Gln181SerfsTer?
ENST00000412368.6:c.*986del (JMJD8) ENSP00000399475.2:n.*986del
ENST00000563505.5:n.637del (STUB1)
ENST00000564316.1:c.140del (STUB1)
ENST00000564370.5:c.325del (STUB1) ENSP00000456875.1:p.Gln109SerfsTer?
ENST00000565302.5:n.1865del (JMJD8)
ENST00000565677.5:c.325del (STUB1) ENSP00000457228.1:p.Gln109SerfsTer?
ENST00000566181.2:n.310del (STUB1)
ENST00000566408.5:c.258del (STUB1)
ENST00000567120.5:n.2068del (JMJD8)
ENST00000567173.5:c.484del (STUB1) ENSP00000456591.1:p.Gln162SerfsTer?
ENST00000568689.5:n.1889del (JMJD8)
ENST00000569248.5:n.1115del (STUB1)
ENST00000609261.5:c.*986del (JMJD8) ENSP00000477481.1:n.*986del
ENST00000620831.4:c.-50+38506del (MSLN) ENSP00000482893.1:n.-50+38506del
NM_001005920.2:c.*986del (JMJD8) NP_001005920.2:n.*986del
NM_001293197.1:c.325del (STUB1) NP_001280126.1:p.Gln109SerfsTer?
NM_005861.3:c.541del (STUB1) NP_005852.2:p.Gln181SerfsTer?
XM_005255295.3:c.*1020del (JMJD8) XP_005255352.1:n.*1020del
XM_005255297.3:c.*986del (JMJD8) XP_005255354.1:n.*986del
XM_011522474.1:c.*986del (JMJD8) XP_011520776.1:n.*986del
NM_001005920.3:c.*986del (JMJD8) NP_001005920.3:n.*986del
NM_001323918.2:c.*1020del (JMJD8) NP_001310847.2:n.*1020del
NM_001323919.2:c.*986del (JMJD8) NP_001310848.2:n.*986del
NM_001323920.2:c.*986del (JMJD8) NP_001310849.2:n.*986del
NM_001323922.2:c.*1020del (JMJD8) NP_001310851.2:n.*1020del
NR_136650.2:n.1879del (JMJD8)
NR_136651.2:n.1884del (JMJD8)
NR_136652.2:n.1794del (JMJD8)
NM_001005920.4:c.*986del (JMJD8) MANE Select NP_001005920.3:n.*986del
NM_005861.4:c.541del (STUB1) MANE Select NP_005852.2:p.Gln181SerfsTer?
NM_001293197.2:c.325del (STUB1) NP_001280126.1:p.Gln109SerfsTer?
NM_001323918.3:c.*1020del (JMJD8) NP_001310847.2:n.*1020del
NM_001323919.3:c.*986del (JMJD8) NP_001310848.2:n.*986del
NM_001323920.3:c.*986del (JMJD8) NP_001310849.2:n.*986del
NM_001323922.3:c.*1020del (JMJD8) NP_001310851.2:n.*1020del
NR_136650.3:n.1879del (JMJD8)
NR_136651.3:n.1884del (JMJD8)
NR_136652.3:n.1794del (JMJD8)