Canonical Allele Identifier: CA379786871
Gene: OTOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17642184G>C , CM000673.2:g.17642184G>C GRCh38
NC_000011.9:g.17663731G>C , CM000673.1:g.17663731G>C GRCh37
NC_000011.8:g.17620307G>C NCBI36
NG_033191.1:g.99812G>C
NG_033191.2:g.99812G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.8389G>C ENSP00000382323.2:p.Gly2797Arg
ENST00000399397.6:c.8353G>C MANE Select ENSP00000382329.2:p.Gly2785Arg
ENST00000399391.6:c.8389G>C ENSP00000382323.2:p.Gly2797Arg
ENST00000399397.5:c.8353G>C ENSP00000382329.2:p.Gly2785Arg
NM_001277269.1:c.8389G>C NP_001264198.1:p.Gly2797Arg
NM_001292063.1:c.8353G>C NP_001278992.1:p.Gly2785Arg
NM_001277269.2:c.8389G>C NP_001264198.1:p.Gly2797Arg
NM_001292063.2:c.8353G>C MANE Select NP_001278992.1:p.Gly2785Arg