Canonical Allele Identifier: CA1955205818
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17570144_17570147delinsAGGT , CM000673.2:g.17570144_17570147delinsAGGT GRCh38
NC_000011.9:g.17591691_17591694delinsAGGT , CM000673.1:g.17591691_17591694delinsAGGT GRCh37
NC_000011.8:g.17548267_17548270delinsAGGT NCBI36
NG_033191.1:g.27772_27775delinsAGGT
NG_033191.2:g.27772_27775delinsAGGT

Transcript Alleles

HGVS Amino-acid change
ENST00000399391.7:c.1814-69_1814-66delinsAGGT ENSP00000382323.2:n.1814-69_1814-66delins...
ENST00000399397.6:c.1778-69_1778-66delinsAGGT MANE Select ENSP00000382329.2:n.1778-69_1778-66delins...
ENST00000399391.6:c.1814-69_1814-66delinsAGGT ENSP00000382323.2:n.1814-69_1814-66delins...
ENST00000399397.5:c.1778-69_1778-66delinsAGGT ENSP00000382329.2:n.1778-69_1778-66delins...
ENST00000498332.5:n.1684-69_1684-66delinsAGGT
NM_001277269.1:c.1814-69_1814-66delinsAGGT NP_001264198.1:n.1814-69_1814-66delinsAGG...
NM_001292063.1:c.1778-69_1778-66delinsAGGT NP_001278992.1:n.1778-69_1778-66delinsAGG...
NM_001277269.2:c.1814-69_1814-66delinsAGGT NP_001264198.1:n.1814-69_1814-66delinsAGG...
NM_001292063.2:c.1778-69_1778-66delinsAGGT MANE Select NP_001278992.1:n.1778-69_1778-66delinsAGG...