Canonical Allele Identifier: CA2201204924

Gene: STUB1 JMJD8 MSLN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.681829_681832delinsTGAG , CM000678.2:g.681829_681832delinsTGAG	GRCh38
NC_000016.9:g.731829_731832delinsTGAG , CM000678.1:g.731829_731832delinsTGAG	GRCh37
NC_000016.8:g.671830_671833delinsTGAG	NCBI36
NG_034141.1:g.6719_6722delinsTGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219548.9:c.561_564delinsTGAG (STUB1) MANE Select	ENSP00000219548.4:p.Asp187=
ENST00000609261.6:c.*962_*965delinsCTCA (JMJD8) MANE Select	ENSP00000477481.1:n.*962_*965delinsCTCA
ENST00000219548.8:c.561_564delinsTGAG (STUB1)	ENSP00000219548.4:p.Asp187=
ENST00000412368.6:c.*962_*965delinsCTCA (JMJD8)	ENSP00000399475.2:n.*962_*965delinsCTCA
ENST00000563505.5:n.657_660delinsTGAG (STUB1)
ENST00000564316.1:c.160_163delinsTGAG (STUB1)
ENST00000564370.5:c.345_348delinsTGAG (STUB1)	ENSP00000456875.1:p.Asp115=
ENST00000565302.5:n.1841_1844delinsCTCA (JMJD8)
ENST00000565677.5:c.345_348delinsTGAG (STUB1)	ENSP00000457228.1:p.Asp115=
ENST00000566181.2:n.330_333delinsTGAG (STUB1)
ENST00000566408.5:c.278_281delinsTGAG (STUB1)
ENST00000567120.5:n.2044_2047delinsCTCA (JMJD8)
ENST00000567173.5:c.504_507delinsTGAG (STUB1)	ENSP00000456591.1:p.Asp168=
ENST00000568689.5:n.1865_1868delinsCTCA (JMJD8)
ENST00000569248.5:n.1135_1138delinsTGAG (STUB1)
ENST00000609261.5:c.*962_*965delinsCTCA (JMJD8)	ENSP00000477481.1:n.*962_*965delinsCTCA
ENST00000620831.4:c.-50+38526_-50+38529delinsTGAG (MSLN)	ENSP00000482893.1:n.-50+38526_-50+38529delinsTGAG
NM_001005920.2:c.*962_*965delinsCTCA (JMJD8)	NP_001005920.2:n.*962_*965delinsCTCA
NM_001293197.1:c.345_348delinsTGAG (STUB1)	NP_001280126.1:p.Asp115=
NM_005861.3:c.561_564delinsTGAG (STUB1)	NP_005852.2:p.Asp187=
XM_005255295.3:c.*996_*999delinsCTCA (JMJD8)	XP_005255352.1:n.*996_*999delinsCTCA
XM_005255297.3:c.*962_*965delinsCTCA (JMJD8)	XP_005255354.1:n.*962_*965delinsCTCA
XM_011522474.1:c.*962_*965delinsCTCA (JMJD8)	XP_011520776.1:n.*962_*965delinsCTCA
NM_001005920.3:c.*962_*965delinsCTCA (JMJD8)	NP_001005920.3:n.*962_*965delinsCTCA
NM_001323918.2:c.*996_*999delinsCTCA (JMJD8)	NP_001310847.2:n.*996_*999delinsCTCA
NM_001323919.2:c.*962_*965delinsCTCA (JMJD8)	NP_001310848.2:n.*962_*965delinsCTCA
NM_001323920.2:c.*962_*965delinsCTCA (JMJD8)	NP_001310849.2:n.*962_*965delinsCTCA
NM_001323922.2:c.*996_*999delinsCTCA (JMJD8)	NP_001310851.2:n.*996_*999delinsCTCA
NR_136650.2:n.1855_1858delinsCTCA (JMJD8)
NR_136651.2:n.1860_1863delinsCTCA (JMJD8)
NR_136652.2:n.1770_1773delinsCTCA (JMJD8)
NM_001005920.4:c.*962_*965delinsCTCA (JMJD8) MANE Select	NP_001005920.3:n.*962_*965delinsCTCA
NM_005861.4:c.561_564delinsTGAG (STUB1) MANE Select	NP_005852.2:p.Asp187=
NM_001293197.2:c.345_348delinsTGAG (STUB1)	NP_001280126.1:p.Asp115=
NM_001323918.3:c.*996_*999delinsCTCA (JMJD8)	NP_001310847.2:n.*996_*999delinsCTCA
NM_001323919.3:c.*962_*965delinsCTCA (JMJD8)	NP_001310848.2:n.*962_*965delinsCTCA
NM_001323920.3:c.*962_*965delinsCTCA (JMJD8)	NP_001310849.2:n.*962_*965delinsCTCA
NM_001323922.3:c.*996_*999delinsCTCA (JMJD8)	NP_001310851.2:n.*996_*999delinsCTCA
NR_136650.3:n.1855_1858delinsCTCA (JMJD8)
NR_136651.3:n.1860_1863delinsCTCA (JMJD8)
NR_136652.3:n.1770_1773delinsCTCA (JMJD8)