Canonical Allele Identifier: CA1955232938

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17612404_17612406delinsCTG , CM000673.2:g.17612404_17612406delinsCTG	GRCh38
NC_000011.9:g.17633951_17633953delinsCTG , CM000673.1:g.17633951_17633953delinsCTG	GRCh37
NC_000011.8:g.17590527_17590529delinsCTG	NCBI36
NG_033191.1:g.70032_70034delinsCTG
NG_033191.2:g.70032_70034delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.6328+74_6328+76delinsCTG	ENSP00000382323.2:n.6328+74_6328+76delinsCTG
ENST00000399397.6:c.6292+74_6292+76delinsCTG MANE Select	ENSP00000382329.2:n.6292+74_6292+76delinsCTG
ENST00000342528.2:c.3346+74_3346+76delinsCTG	ENSP00000341666.2:n.3346+74_3346+76delinsCTG
ENST00000399391.6:c.6328+74_6328+76delinsCTG	ENSP00000382323.2:n.6328+74_6328+76delinsCTG
ENST00000399397.5:c.6292+74_6292+76delinsCTG	ENSP00000382329.2:n.6292+74_6292+76delinsCTG
NM_001277269.1:c.6328+74_6328+76delinsCTG	NP_001264198.1:n.6328+74_6328+76delinsCTG
NM_001292063.1:c.6292+74_6292+76delinsCTG	NP_001278992.1:n.6292+74_6292+76delinsCTG
NM_001277269.2:c.6328+74_6328+76delinsCTG	NP_001264198.1:n.6328+74_6328+76delinsCTG
NM_001292063.2:c.6292+74_6292+76delinsCTG MANE Select	NP_001278992.1:n.6292+74_6292+76delinsCTG