Canonical Allele Identifier: CA1955197786
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553470A= , CM000673.2:g.17553470A= GRCh38
NC_000011.9:g.17575017A= , CM000673.1:g.17575017A= GRCh37
NC_000011.8:g.17531593A= NCBI36
NG_033191.1:g.11098A=
NG_033191.2:g.11098A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.527A= ENSP00000382323.2:p.Tyr176=
ENST00000399397.6:c.491A= MANE Select ENSP00000382329.2:p.Tyr164=
ENST00000399391.6:c.527A= ENSP00000382323.2:p.Tyr176=
ENST00000399397.5:c.491A= ENSP00000382329.2:p.Tyr164=
ENST00000498332.5:n.397A=
NM_001277269.1:c.527A= NP_001264198.1:p.Tyr176=
NM_001292063.1:c.491A= NP_001278992.1:p.Tyr164=
NM_001277269.2:c.527A= NP_001264198.1:p.Tyr176=
NM_001292063.2:c.491A= MANE Select NP_001278992.1:p.Tyr164=