Canonical Allele Identifier: CA371657682

Gene: OTUD6B

Linked Data

• MyVariant Identifiers: chr8:g.92083374C>A (hg19) ; chr8:g.91071146C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.91071146C>A , CM000670.2:g.91071146C>A	GRCh38
NC_000008.10:g.92083374C>A , CM000670.1:g.92083374C>A	GRCh37
NC_000008.9:g.92152550C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000404789.8:c.91C>A MANE Select	ENSP00000384190.4:p.Gln31Lys
ENST00000285420.8:c.181C>A	ENSP00000285420.4:p.Gln61Lys
ENST00000404789.7:c.91C>A	ENSP00000384190.4:p.Gln31Lys
ENST00000522894.5:c.91C>A	ENSP00000428528.2:p.Gln31Lys
ENST00000524027.5:n.114C>A
ENST00000615618.1:c.-353C>A	ENSP00000481196.1:n.-353C>A
ENST00000617869.4:c.181C>A	ENSP00000483706.1:p.Gln61Lys
NM_001286745.1:c.-353C>A	NP_001273674.1:n.-353C>A
NM_016023.3:c.181C>A	NP_057107.3:p.Gln61Lys
XM_011517129.1:c.181C>A	XP_011515431.1:p.Gln61Lys
NM_001286745.2:c.-353C>A	NP_001273674.1:n.-353C>A
NM_016023.4:c.91C>A	NP_057107.4:p.Gln31Lys
XM_011517129.2:c.-349C>A	XP_011515431.2:n.-349C>A
NM_016023.5:c.91C>A MANE Select	NP_057107.4:p.Gln31Lys
NM_001286745.3:c.-353C>A	NP_001273674.1:n.-353C>A