Canonical Allele Identifier: CA10663367

Gene: OTUD3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19901230G>C , CM000663.2:g.19901230G>C	GRCh38
NC_000001.10:g.20227723G>C , CM000663.1:g.20227723G>C	GRCh37
NC_000001.9:g.20100310G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375120.4:c.607-3037G>C MANE Select	ENSP00000364261.3:n.607-3037G>C
ENST00000375120.3:c.607-3037G>C	ENSP00000364261.3:n.607-3037G>C
NM_015207.1:c.607-3037G>C	NP_056022.1:n.607-3037G>C
XM_005245792.2:c.832-3037G>C	XP_005245849.1:n.832-3037G>C
XM_005245793.2:c.832-3037G>C	XP_005245850.1:n.832-3037G>C
XM_005245794.2:c.148-3037G>C	XP_005245851.1:n.148-3037G>C
XM_011541071.1:c.424-3037G>C	XP_011539373.1:n.424-3037G>C
XM_011541072.1:c.301-3037G>C	XP_011539374.1:n.301-3037G>C
XM_011541073.1:c.301-3037G>C	XP_011539375.1:n.301-3037G>C
XM_005245792.4:c.832-3037G>C	XP_005245849.1:n.832-3037G>C
XM_005245793.4:c.832-3037G>C	XP_005245850.1:n.832-3037G>C
XM_005245794.3:c.148-3037G>C	XP_005245851.1:n.148-3037G>C
XM_024454320.1:c.301-3037G>C	XP_024310088.1:n.301-3037G>C
NM_015207.2:c.607-3037G>C MANE Select	NP_056022.1:n.607-3037G>C