Canonical Allele Identifier: CA371657673

Gene: OTUD6B

Linked Data

• MyVariant Identifiers: chr8:g.92083370A>T (hg19) ; chr8:g.91071142A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.91071142A>T , CM000670.2:g.91071142A>T	GRCh38
NC_000008.10:g.92083370A>T , CM000670.1:g.92083370A>T	GRCh37
NC_000008.9:g.92152546A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000404789.8:c.87A>T MANE Select	ENSP00000384190.4:p.Lys29Asn
ENST00000285420.8:c.177A>T	ENSP00000285420.4:p.Lys59Asn
ENST00000404789.7:c.87A>T	ENSP00000384190.4:p.Lys29Asn
ENST00000522894.5:c.87A>T	ENSP00000428528.2:p.Lys29Asn
ENST00000524027.5:n.110A>T
ENST00000615618.1:c.-357A>T	ENSP00000481196.1:n.-357A>T
ENST00000617869.4:c.177A>T	ENSP00000483706.1:p.Lys59Asn
NM_001286745.1:c.-357A>T	NP_001273674.1:n.-357A>T
NM_016023.3:c.177A>T	NP_057107.3:p.Lys59Asn
XM_011517129.1:c.177A>T	XP_011515431.1:p.Lys59Asn
NM_001286745.2:c.-357A>T	NP_001273674.1:n.-357A>T
NM_016023.4:c.87A>T	NP_057107.4:p.Lys29Asn
XM_011517129.2:c.-353A>T	XP_011515431.2:n.-353A>T
NM_016023.5:c.87A>T MANE Select	NP_057107.4:p.Lys29Asn
NM_001286745.3:c.-357A>T	NP_001273674.1:n.-357A>T