Canonical Allele Identifier: CA1955197542
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553016G= , CM000673.2:g.17553016G= GRCh38
NC_000011.9:g.17574563G= , CM000673.1:g.17574563G= GRCh37
NC_000011.8:g.17531139G= NCBI36
NG_033191.1:g.10644G=
NG_033191.2:g.10644G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.329-103G= ENSP00000382323.2:n.329-103G=
ENST00000399397.6:c.293-103G= MANE Select ENSP00000382329.2:n.293-103G=
ENST00000399391.6:c.329-103G= ENSP00000382323.2:n.329-103G=
ENST00000399397.5:c.293-103G= ENSP00000382329.2:n.293-103G=
ENST00000428619.1:c.110-103G= ENSP00000399057.2:n.110-103G=
ENST00000498332.5:n.199-103G=
NM_001277269.1:c.329-103G= NP_001264198.1:n.329-103G=
NM_001292063.1:c.293-103G= NP_001278992.1:n.293-103G=
NM_001277269.2:c.329-103G= NP_001264198.1:n.329-103G=
NM_001292063.2:c.293-103G= MANE Select NP_001278992.1:n.293-103G=