Canonical Allele Identifier: CA394112806

Gene: STUB1 JMJD8 MSLN

Linked Data

• gnomAD v4: 16-681797-C-A
• MyVariant Identifiers: chr16:g.731797C>A (hg19) ; chr16:g.681797C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.681797C>A , CM000678.2:g.681797C>A	GRCh38
NC_000016.9:g.731797C>A , CM000678.1:g.731797C>A	GRCh37
NC_000016.8:g.671798C>A	NCBI36
NG_034141.1:g.6687C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219548.9:c.529C>A (STUB1) MANE Select	ENSP00000219548.4:p.Leu177Met
ENST00000609261.6:c.*997G>T (JMJD8) MANE Select	ENSP00000477481.1:n.*997G>T
ENST00000219548.8:c.529C>A (STUB1)	ENSP00000219548.4:p.Leu177Met
ENST00000412368.6:c.*997G>T (JMJD8)	ENSP00000399475.2:n.*997G>T
ENST00000563505.5:n.625C>A (STUB1)
ENST00000564316.1:c.128C>A (STUB1)
ENST00000564370.5:c.313C>A (STUB1)	ENSP00000456875.1:p.Leu105Met
ENST00000565302.5:n.1876G>T (JMJD8)
ENST00000565677.5:c.313C>A (STUB1)	ENSP00000457228.1:p.Leu105Met
ENST00000566181.2:n.298C>A (STUB1)
ENST00000566408.5:c.246C>A (STUB1)
ENST00000567120.5:n.2079G>T (JMJD8)
ENST00000567173.5:c.472C>A (STUB1)	ENSP00000456591.1:p.Leu158Met
ENST00000568689.5:n.1900G>T (JMJD8)
ENST00000569248.5:n.1103C>A (STUB1)
ENST00000609261.5:c.*997G>T (JMJD8)	ENSP00000477481.1:n.*997G>T
ENST00000620831.4:c.-50+38494C>A (MSLN)	ENSP00000482893.1:n.-50+38494C>A
NM_001005920.2:c.*997G>T (JMJD8)	NP_001005920.2:n.*997G>T
NM_001293197.1:c.313C>A (STUB1)	NP_001280126.1:p.Leu105Met
NM_005861.3:c.529C>A (STUB1)	NP_005852.2:p.Leu177Met
XM_005255295.3:c.*1031G>T (JMJD8)	XP_005255352.1:n.*1031G>T
XM_005255297.3:c.*997G>T (JMJD8)	XP_005255354.1:n.*997G>T
XM_011522474.1:c.*997G>T (JMJD8)	XP_011520776.1:n.*997G>T
NM_001005920.3:c.*997G>T (JMJD8)	NP_001005920.3:n.*997G>T
NM_001323918.2:c.*1031G>T (JMJD8)	NP_001310847.2:n.*1031G>T
NM_001323919.2:c.*997G>T (JMJD8)	NP_001310848.2:n.*997G>T
NM_001323920.2:c.*997G>T (JMJD8)	NP_001310849.2:n.*997G>T
NM_001323922.2:c.*1031G>T (JMJD8)	NP_001310851.2:n.*1031G>T
NR_136650.2:n.1890G>T (JMJD8)
NR_136651.2:n.1895G>T (JMJD8)
NR_136652.2:n.1805G>T (JMJD8)
NM_001005920.4:c.*997G>T (JMJD8) MANE Select	NP_001005920.3:n.*997G>T
NM_005861.4:c.529C>A (STUB1) MANE Select	NP_005852.2:p.Leu177Met
NM_001293197.2:c.313C>A (STUB1)	NP_001280126.1:p.Leu105Met
NM_001323918.3:c.*1031G>T (JMJD8)	NP_001310847.2:n.*1031G>T
NM_001323919.3:c.*997G>T (JMJD8)	NP_001310848.2:n.*997G>T
NM_001323920.3:c.*997G>T (JMJD8)	NP_001310849.2:n.*997G>T
NM_001323922.3:c.*1031G>T (JMJD8)	NP_001310851.2:n.*1031G>T
NR_136650.3:n.1890G>T (JMJD8)
NR_136651.3:n.1895G>T (JMJD8)
NR_136652.3:n.1805G>T (JMJD8)