Canonical Allele Identifier: CA1955242287
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17645748A= , CM000673.2:g.17645748A= GRCh38
NC_000011.9:g.17667295A= , CM000673.1:g.17667295A= GRCh37
NC_000011.8:g.17623871A= NCBI36
NG_033191.1:g.103376A=
NG_033191.2:g.103376A=

Transcript Alleles

HGVS Amino-acid change
ENST00000399391.7:c.8582A= ENSP00000382323.2:p.Asn2861=
ENST00000399397.6:c.8546A= MANE Select ENSP00000382329.2:p.Asn2849=
ENST00000399391.6:c.8582A= ENSP00000382323.2:p.Asn2861=
ENST00000399397.5:c.8546A= ENSP00000382329.2:p.Asn2849=
NM_001277269.1:c.8582A= NP_001264198.1:p.Asn2861=
NM_001292063.1:c.8546A= NP_001278992.1:p.Asn2849=
NM_001277269.2:c.8582A= NP_001264198.1:p.Asn2861=
NM_001292063.2:c.8546A= MANE Select NP_001278992.1:p.Asn2849=