Canonical Allele Identifier: CA2612687141

Gene: OTOG

Linked Data

• gnomAD v4: 11-17612856-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17612859del , CM000673.2:g.17612859del	GRCh38
NC_000011.9:g.17634406del , CM000673.1:g.17634406del	GRCh37
NC_000011.8:g.17590982del	NCBI36
NG_033191.1:g.70487del
NG_033191.2:g.70487del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.6474+94del	ENSP00000382323.2:n.6474+94del
ENST00000399397.6:c.6438+94del MANE Select	ENSP00000382329.2:n.6438+94del
ENST00000342528.2:c.3492+94del	ENSP00000341666.2:n.3492+94del
ENST00000399391.6:c.6474+94del	ENSP00000382323.2:n.6474+94del
ENST00000399397.5:c.6438+94del	ENSP00000382329.2:n.6438+94del
NM_001277269.1:c.6474+94del	NP_001264198.1:n.6474+94del
NM_001292063.1:c.6438+94del	NP_001278992.1:n.6438+94del
NM_001277269.2:c.6474+94del	NP_001264198.1:n.6474+94del
NM_001292063.2:c.6438+94del MANE Select	NP_001278992.1:n.6438+94del