Canonical Allele Identifier: CA7786659

Gene: STUB1 JMJD8 MSLN

Linked Data

• ClinVar Variation Id: 1980459
• ClinVar RCV Id: RCV002780251
• dbSNP Id: rs145094142
• ExAC: 16:731813 G / A
• gnomAD v2: 16-731813-G-A
• gnomAD v3: 16-681813-G-A
• gnomAD v4: 16-681813-G-A
• MyVariant Identifiers: chr16:g.731813G>A (hg19) ; chr16:g.681813G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.681813G>A , CM000678.2:g.681813G>A	GRCh38
NC_000016.9:g.731813G>A , CM000678.1:g.731813G>A	GRCh37
NC_000016.8:g.671814G>A	NCBI36
NG_034141.1:g.6703G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219548.9:c.545G>A (STUB1) MANE Select	ENSP00000219548.4:p.Arg182Gln
ENST00000609261.6:c.*981C>T (JMJD8) MANE Select	ENSP00000477481.1:n.*981C>T
ENST00000219548.8:c.545G>A (STUB1)	ENSP00000219548.4:p.Arg182Gln
ENST00000412368.6:c.*981C>T (JMJD8)	ENSP00000399475.2:n.*981C>T
ENST00000563505.5:n.641G>A (STUB1)
ENST00000564316.1:c.144G>A (STUB1)
ENST00000564370.5:c.329G>A (STUB1)	ENSP00000456875.1:p.Arg110Gln
ENST00000565302.5:n.1860C>T (JMJD8)
ENST00000565677.5:c.329G>A (STUB1)	ENSP00000457228.1:p.Arg110Gln
ENST00000566181.2:n.314G>A (STUB1)
ENST00000566408.5:c.262G>A (STUB1)
ENST00000567120.5:n.2063C>T (JMJD8)
ENST00000567173.5:c.488G>A (STUB1)	ENSP00000456591.1:p.Arg163Gln
ENST00000568689.5:n.1884C>T (JMJD8)
ENST00000569248.5:n.1119G>A (STUB1)
ENST00000609261.5:c.*981C>T (JMJD8)	ENSP00000477481.1:n.*981C>T
ENST00000620831.4:c.-50+38510G>A (MSLN)	ENSP00000482893.1:n.-50+38510G>A
NM_001005920.2:c.*981C>T (JMJD8)	NP_001005920.2:n.*981C>T
NM_001293197.1:c.329G>A (STUB1)	NP_001280126.1:p.Arg110Gln
NM_005861.3:c.545G>A (STUB1)	NP_005852.2:p.Arg182Gln
XM_005255295.3:c.*1015C>T (JMJD8)	XP_005255352.1:n.*1015C>T
XM_005255297.3:c.*981C>T (JMJD8)	XP_005255354.1:n.*981C>T
XM_011522474.1:c.*981C>T (JMJD8)	XP_011520776.1:n.*981C>T
NM_001005920.3:c.*981C>T (JMJD8)	NP_001005920.3:n.*981C>T
NM_001323918.2:c.*1015C>T (JMJD8)	NP_001310847.2:n.*1015C>T
NM_001323919.2:c.*981C>T (JMJD8)	NP_001310848.2:n.*981C>T
NM_001323920.2:c.*981C>T (JMJD8)	NP_001310849.2:n.*981C>T
NM_001323922.2:c.*1015C>T (JMJD8)	NP_001310851.2:n.*1015C>T
NR_136650.2:n.1874C>T (JMJD8)
NR_136651.2:n.1879C>T (JMJD8)
NR_136652.2:n.1789C>T (JMJD8)
NM_001005920.4:c.*981C>T (JMJD8) MANE Select	NP_001005920.3:n.*981C>T
NM_005861.4:c.545G>A (STUB1) MANE Select	NP_005852.2:p.Arg182Gln
NM_001293197.2:c.329G>A (STUB1)	NP_001280126.1:p.Arg110Gln
NM_001323918.3:c.*1015C>T (JMJD8)	NP_001310847.2:n.*1015C>T
NM_001323919.3:c.*981C>T (JMJD8)	NP_001310848.2:n.*981C>T
NM_001323920.3:c.*981C>T (JMJD8)	NP_001310849.2:n.*981C>T
NM_001323922.3:c.*1015C>T (JMJD8)	NP_001310851.2:n.*1015C>T
NR_136650.3:n.1874C>T (JMJD8)
NR_136651.3:n.1879C>T (JMJD8)
NR_136652.3:n.1789C>T (JMJD8)