Canonical Allele Identifier: CA218454563

Gene: OTOG

Linked Data

• dbSNP Id: rs752615542
• MyVariant Identifiers: chr11:g.17659993_17659994del (hg19) ; chr11:g.17638446_17638447del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17638448_17638449del , CM000673.2:g.17638448_17638449del	GRCh38
NC_000011.9:g.17659995_17659996del , CM000673.1:g.17659995_17659996del	GRCh37
NC_000011.8:g.17616571_17616572del	NCBI36
NG_033191.1:g.96076_96077del
NG_033191.2:g.96076_96077del

Transcript Alleles

HGVS	Amino-acid change
ENST00000399391.7:c.7832-3_7832-2del	ENSP00000382323.2:n.7832-3_7832-2del
ENST00000399397.6:c.7796-3_7796-2del MANE Select	ENSP00000382329.2:n.7796-3_7796-2del
ENST00000342528.2:c.4424-3_4424-2del	ENSP00000341666.2:n.4424-3_4424-2del
ENST00000399391.6:c.7832-3_7832-2del	ENSP00000382323.2:n.7832-3_7832-2del
ENST00000399397.5:c.7796-3_7796-2del	ENSP00000382329.2:n.7796-3_7796-2del
NM_001277269.1:c.7832-3_7832-2del	NP_001264198.1:n.7832-3_7832-2del
NM_001292063.1:c.7796-3_7796-2del	NP_001278992.1:n.7796-3_7796-2del
NM_001277269.2:c.7832-3_7832-2del	NP_001264198.1:n.7832-3_7832-2del
NM_001292063.2:c.7796-3_7796-2del MANE Select	NP_001278992.1:n.7796-3_7796-2del