Canonical Allele Identifier: CA379811804
Gene: OTOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553490G>T , CM000673.2:g.17553490G>T GRCh38
NC_000011.9:g.17575037G>T , CM000673.1:g.17575037G>T GRCh37
NC_000011.8:g.17531613G>T NCBI36
NG_033191.1:g.11118G>T
NG_033191.2:g.11118G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000399391.7:c.547G>T ENSP00000382323.2:p.Glu183Ter
ENST00000399397.6:c.511G>T MANE Select ENSP00000382329.2:p.Glu171Ter
ENST00000399391.6:c.547G>T ENSP00000382323.2:p.Glu183Ter
ENST00000399397.5:c.511G>T ENSP00000382329.2:p.Glu171Ter
ENST00000498332.5:n.417G>T
NM_001277269.1:c.547G>T NP_001264198.1:p.Glu183Ter
NM_001292063.1:c.511G>T NP_001278992.1:p.Glu171Ter
NM_001277269.2:c.547G>T NP_001264198.1:p.Glu183Ter
NM_001292063.2:c.511G>T MANE Select NP_001278992.1:p.Glu171Ter