Canonical Allele Identifier: CA1955232947
Gene: OTOG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17612422C= , CM000673.2:g.17612422C= GRCh38
NC_000011.9:g.17633969C= , CM000673.1:g.17633969C= GRCh37
NC_000011.8:g.17590545C= NCBI36
NG_033191.1:g.70050C=
NG_033191.2:g.70050C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.6328+92C= ENSP00000382323.2:n.6328+92C=
ENST00000399397.6:c.6292+92C= MANE Select ENSP00000382329.2:n.6292+92C=
ENST00000342528.2:c.3346+92C= ENSP00000341666.2:n.3346+92C=
ENST00000399391.6:c.6328+92C= ENSP00000382323.2:n.6328+92C=
ENST00000399397.5:c.6292+92C= ENSP00000382329.2:n.6292+92C=
NM_001277269.1:c.6328+92C= NP_001264198.1:n.6328+92C=
NM_001292063.1:c.6292+92C= NP_001278992.1:n.6292+92C=
NM_001277269.2:c.6328+92C= NP_001264198.1:n.6328+92C=
NM_001292063.2:c.6292+92C= MANE Select NP_001278992.1:n.6292+92C=
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