Canonical Allele Identifier: CA16616848

Gene: OTUD6B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.91078597A>G , CM000670.2:g.91078597A>G	GRCh38
NC_000008.10:g.92090825A>G , CM000670.1:g.92090825A>G	GRCh37
NC_000008.9:g.92160001A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_016023.5:c.557A>G MANE Select	NP_057107.4:p.Tyr186Cys
ENST00000404789.8:c.557A>G MANE Select	ENSP00000384190.4:p.Tyr186Cys
NM_001286745.1:c.254A>G	NP_001273674.1:p.Tyr85Cys
NM_001286745.2:c.254A>G	NP_001273674.1:p.Tyr85Cys
NM_001286745.3:c.254A>G	NP_001273674.1:p.Tyr85Cys
NM_016023.3:c.647A>G	NP_057107.3:p.Tyr216Cys
NM_016023.4:c.557A>G	NP_057107.4:p.Tyr186Cys
ENST00000285420.8:c.647A>G	ENSP00000285420.4:p.Tyr216Cys
ENST00000404789.7:c.557A>G	ENSP00000384190.4:p.Tyr186Cys
ENST00000522894.5:c.*370A>G	ENSP00000428528.2:n.*370A>G
ENST00000524027.5:n.720A>G
ENST00000615618.1:c.254A>G	ENSP00000481196.1:p.Tyr85Cys
ENST00000617869.4:c.647A>G	ENSP00000483706.1:p.Tyr216Cys
XM_011517129.2:c.254A>G	XP_011515431.2:p.Tyr85Cys