Canonical Allele Identifier: CA379811775
Gene: OTOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553478G>T , CM000673.2:g.17553478G>T GRCh38
NC_000011.9:g.17575025G>T , CM000673.1:g.17575025G>T GRCh37
NC_000011.8:g.17531601G>T NCBI36
NG_033191.1:g.11106G>T
NG_033191.2:g.11106G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000399391.7:c.535G>T ENSP00000382323.2:p.Val179Leu
ENST00000399397.6:c.499G>T MANE Select ENSP00000382329.2:p.Val167Leu
ENST00000399391.6:c.535G>T ENSP00000382323.2:p.Val179Leu
ENST00000399397.5:c.499G>T ENSP00000382329.2:p.Val167Leu
ENST00000498332.5:n.405G>T
NM_001277269.1:c.535G>T NP_001264198.1:p.Val179Leu
NM_001292063.1:c.499G>T NP_001278992.1:p.Val167Leu
NM_001277269.2:c.535G>T NP_001264198.1:p.Val179Leu
NM_001292063.2:c.499G>T MANE Select NP_001278992.1:p.Val167Leu