Canonical Allele Identifier: CA394112875

Gene: STUB1 JMJD8 MSLN

Linked Data

• gnomAD v4: 16-681812-C-G
• MyVariant Identifiers: chr16:g.731812C>G (hg19) ; chr16:g.681812C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.681812C>G , CM000678.2:g.681812C>G	GRCh38
NC_000016.9:g.731812C>G , CM000678.1:g.731812C>G	GRCh37
NC_000016.8:g.671813C>G	NCBI36
NG_034141.1:g.6702C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219548.9:c.544C>G (STUB1) MANE Select	ENSP00000219548.4:p.Arg182Gly
ENST00000609261.6:c.*982G>C (JMJD8) MANE Select	ENSP00000477481.1:n.*982G>C
ENST00000219548.8:c.544C>G (STUB1)	ENSP00000219548.4:p.Arg182Gly
ENST00000412368.6:c.*982G>C (JMJD8)	ENSP00000399475.2:n.*982G>C
ENST00000563505.5:n.640C>G (STUB1)
ENST00000564316.1:c.143C>G (STUB1)
ENST00000564370.5:c.328C>G (STUB1)	ENSP00000456875.1:p.Arg110Gly
ENST00000565302.5:n.1861G>C (JMJD8)
ENST00000565677.5:c.328C>G (STUB1)	ENSP00000457228.1:p.Arg110Gly
ENST00000566181.2:n.313C>G (STUB1)
ENST00000566408.5:c.261C>G (STUB1)
ENST00000567120.5:n.2064G>C (JMJD8)
ENST00000567173.5:c.487C>G (STUB1)	ENSP00000456591.1:p.Arg163Gly
ENST00000568689.5:n.1885G>C (JMJD8)
ENST00000569248.5:n.1118C>G (STUB1)
ENST00000609261.5:c.*982G>C (JMJD8)	ENSP00000477481.1:n.*982G>C
ENST00000620831.4:c.-50+38509C>G (MSLN)	ENSP00000482893.1:n.-50+38509C>G
NM_001005920.2:c.*982G>C (JMJD8)	NP_001005920.2:n.*982G>C
NM_001293197.1:c.328C>G (STUB1)	NP_001280126.1:p.Arg110Gly
NM_005861.3:c.544C>G (STUB1)	NP_005852.2:p.Arg182Gly
XM_005255295.3:c.*1016G>C (JMJD8)	XP_005255352.1:n.*1016G>C
XM_005255297.3:c.*982G>C (JMJD8)	XP_005255354.1:n.*982G>C
XM_011522474.1:c.*982G>C (JMJD8)	XP_011520776.1:n.*982G>C
NM_001005920.3:c.*982G>C (JMJD8)	NP_001005920.3:n.*982G>C
NM_001323918.2:c.*1016G>C (JMJD8)	NP_001310847.2:n.*1016G>C
NM_001323919.2:c.*982G>C (JMJD8)	NP_001310848.2:n.*982G>C
NM_001323920.2:c.*982G>C (JMJD8)	NP_001310849.2:n.*982G>C
NM_001323922.2:c.*1016G>C (JMJD8)	NP_001310851.2:n.*1016G>C
NR_136650.2:n.1875G>C (JMJD8)
NR_136651.2:n.1880G>C (JMJD8)
NR_136652.2:n.1790G>C (JMJD8)
NM_001005920.4:c.*982G>C (JMJD8) MANE Select	NP_001005920.3:n.*982G>C
NM_005861.4:c.544C>G (STUB1) MANE Select	NP_005852.2:p.Arg182Gly
NM_001293197.2:c.328C>G (STUB1)	NP_001280126.1:p.Arg110Gly
NM_001323918.3:c.*1016G>C (JMJD8)	NP_001310847.2:n.*1016G>C
NM_001323919.3:c.*982G>C (JMJD8)	NP_001310848.2:n.*982G>C
NM_001323920.3:c.*982G>C (JMJD8)	NP_001310849.2:n.*982G>C
NM_001323922.3:c.*1016G>C (JMJD8)	NP_001310851.2:n.*1016G>C
NR_136650.3:n.1875G>C (JMJD8)
NR_136651.3:n.1880G>C (JMJD8)
NR_136652.3:n.1790G>C (JMJD8)