Canonical Allele Identifier: CA2612681897
Gene: OTOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17570144A>G , CM000673.2:g.17570144A>G GRCh38
NC_000011.9:g.17591691A>G , CM000673.1:g.17591691A>G GRCh37
NC_000011.8:g.17548267A>G NCBI36
NG_033191.1:g.27772A>G
NG_033191.2:g.27772A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000399391.7:c.1814-69A>G ENSP00000382323.2:n.1814-69A>G
ENST00000399397.6:c.1778-69A>G MANE Select ENSP00000382329.2:n.1778-69A>G
ENST00000399391.6:c.1814-69A>G ENSP00000382323.2:n.1814-69A>G
ENST00000399397.5:c.1778-69A>G ENSP00000382329.2:n.1778-69A>G
ENST00000498332.5:n.1684-69A>G
NM_001277269.1:c.1814-69A>G NP_001264198.1:n.1814-69A>G
NM_001292063.1:c.1778-69A>G NP_001278992.1:n.1778-69A>G
NM_001277269.2:c.1814-69A>G NP_001264198.1:n.1814-69A>G
NM_001292063.2:c.1778-69A>G MANE Select NP_001278992.1:n.1778-69A>G