Canonical Allele Identifier: CA1955233029

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17612591_17612594delinsATTC , CM000673.2:g.17612591_17612594delinsATTC	GRCh38
NC_000011.9:g.17634138_17634141delinsATTC , CM000673.1:g.17634138_17634141delinsATTC	GRCh37
NC_000011.8:g.17590714_17590717delinsATTC	NCBI36
NG_033191.1:g.70219_70222delinsATTC
NG_033191.2:g.70219_70222delinsATTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.6329-29_6329-26delinsATTC	ENSP00000382323.2:n.6329-29_6329-26delinsATTC
ENST00000399397.6:c.6293-29_6293-26delinsATTC MANE Select	ENSP00000382329.2:n.6293-29_6293-26delinsATTC
ENST00000342528.2:c.3347-29_3347-26delinsATTC	ENSP00000341666.2:n.3347-29_3347-26delinsATTC
ENST00000399391.6:c.6329-29_6329-26delinsATTC	ENSP00000382323.2:n.6329-29_6329-26delinsATTC
ENST00000399397.5:c.6293-29_6293-26delinsATTC	ENSP00000382329.2:n.6293-29_6293-26delinsATTC
NM_001277269.1:c.6329-29_6329-26delinsATTC	NP_001264198.1:n.6329-29_6329-26delinsATTC
NM_001292063.1:c.6293-29_6293-26delinsATTC	NP_001278992.1:n.6293-29_6293-26delinsATTC
NM_001277269.2:c.6329-29_6329-26delinsATTC	NP_001264198.1:n.6329-29_6329-26delinsATTC
NM_001292063.2:c.6293-29_6293-26delinsATTC MANE Select	NP_001278992.1:n.6293-29_6293-26delinsATTC