Canonical Allele Identifier: CA1955197564
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553052_17553053delinsAG , CM000673.2:g.17553052_17553053delinsAG GRCh38
NC_000011.9:g.17574599_17574600delinsAG , CM000673.1:g.17574599_17574600delinsAG GRCh37
NC_000011.8:g.17531175_17531176delinsAG NCBI36
NG_033191.1:g.10680_10681delinsAG
NG_033191.2:g.10680_10681delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.329-67_329-66delinsAG ENSP00000382323.2:n.329-67_329-66delinsAG
ENST00000399397.6:c.293-67_293-66delinsAG MANE Select ENSP00000382329.2:n.293-67_293-66delinsAG
ENST00000399391.6:c.329-67_329-66delinsAG ENSP00000382323.2:n.329-67_329-66delinsAG
ENST00000399397.5:c.293-67_293-66delinsAG ENSP00000382329.2:n.293-67_293-66delinsAG
ENST00000428619.1:c.110-67_110-66delinsAG ENSP00000399057.2:n.110-67_110-66delinsAG
ENST00000498332.5:n.199-67_199-66delinsAG
NM_001277269.1:c.329-67_329-66delinsAG NP_001264198.1:n.329-67_329-66delinsAG
NM_001292063.1:c.293-67_293-66delinsAG NP_001278992.1:n.293-67_293-66delinsAG
NM_001277269.2:c.329-67_329-66delinsAG NP_001264198.1:n.329-67_329-66delinsAG
NM_001292063.2:c.293-67_293-66delinsAG MANE Select NP_001278992.1:n.293-67_293-66delinsAG