Canonical Allele Identifier: CA2612687069

Gene: OTOG

Linked Data

• gnomAD v4: 11-17612818-A-AAGAGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17612822_17612828dup , CM000673.2:g.17612822_17612828dup	GRCh38
NC_000011.9:g.17634369_17634375dup , CM000673.1:g.17634369_17634375dup	GRCh37
NC_000011.8:g.17590945_17590951dup	NCBI36
NG_033191.1:g.70450_70456dup
NG_033191.2:g.70450_70456dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.6474+57_6474+63dup	ENSP00000382323.2:n.6474+57_6474+63dup
ENST00000399397.6:c.6438+57_6438+63dup MANE Select	ENSP00000382329.2:n.6438+57_6438+63dup
ENST00000342528.2:c.3492+57_3492+63dup	ENSP00000341666.2:n.3492+57_3492+63dup
ENST00000399391.6:c.6474+57_6474+63dup	ENSP00000382323.2:n.6474+57_6474+63dup
ENST00000399397.5:c.6438+57_6438+63dup	ENSP00000382329.2:n.6438+57_6438+63dup
NM_001277269.1:c.6474+57_6474+63dup	NP_001264198.1:n.6474+57_6474+63dup
NM_001292063.1:c.6438+57_6438+63dup	NP_001278992.1:n.6438+57_6438+63dup
NM_001277269.2:c.6474+57_6474+63dup	NP_001264198.1:n.6474+57_6474+63dup
NM_001292063.2:c.6438+57_6438+63dup MANE Select	NP_001278992.1:n.6438+57_6438+63dup