Canonical Allele Identifier: CA199649
Gene: OTX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 190251
dbSNP Id: rs786205224

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.56804202C>T , CM000676.2:g.56804202C>T GRCh38
NC_000014.8:g.57270920C>T , CM000676.1:g.57270920C>T GRCh37
NC_000014.7:g.56340673C>T NCBI36
NG_008204.1:g.11265G>A
NG_008204.2:g.17492G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000554845.2:c.259G>A ENSP00000451357.2:p.Glu87Lys
ENST00000555804.2:c.235G>A ENSP00000451272.2:p.Glu79Lys
ENST00000685244.1:c.235G>A ENSP00000508798.1:p.Glu79Lys
ENST00000339475.10:c.235G>A ENSP00000343819.5:p.Glu79Lys
ENST00000408990.8:c.235G>A ENSP00000386185.3:p.Glu79Lys
ENST00000672125.1:c.235G>A ENSP00000500744.1:p.Glu79Lys
ENST00000672264.2:c.259G>A MANE Select ENSP00000500115.1:p.Glu87Lys
ENST00000673035.1:c.235G>A ENSP00000500061.1:p.Glu79Lys
ENST00000673481.1:c.259G>A ENSP00000500595.1:p.Glu87Lys
ENST00000339475.9:c.259G>A ENSP00000343819.4:p.Glu87Lys
ENST00000408990.7:c.235G>A ENSP00000386185.3:p.Glu79Lys
ENST00000554559.5:c.97+1158G>A ENSP00000450468.1:n.97+1158G>A
ENST00000554788.5:c.97+1158G>A ENSP00000474486.1:n.97+1158G>A
ENST00000554845.1:c.259G>A ENSP00000451357.1:p.Glu87Lys
ENST00000555006.5:c.235G>A ENSP00000452336.1:p.Glu79Lys
ENST00000555804.1:c.235G>A ENSP00000451272.1:p.Glu79Lys
NM_001270523.1:c.235G>A NP_001257452.1:p.Glu79Lys
NM_001270524.1:c.235G>A NP_001257453.1:p.Glu79Lys
NM_001270525.1:c.259G>A NP_001257454.1:p.Glu87Lys
NM_021728.3:c.259G>A NP_068374.1:p.Glu87Lys
NM_172337.2:c.235G>A NP_758840.1:p.Glu79Lys
NR_073034.1:n.381+1158G>A
NR_073036.1:n.304+1158G>A
NM_001270523.2:c.235G>A NP_001257452.1:p.Glu79Lys
NM_001270524.2:c.235G>A NP_001257453.1:p.Glu79Lys
NM_001270525.2:c.259G>A NP_001257454.1:p.Glu87Lys
NM_021728.4:c.259G>A MANE Select NP_068374.1:p.Glu87Lys
NM_172337.3:c.235G>A NP_758840.1:p.Glu79Lys
NR_073034.2:n.384+1158G>A
NR_073036.2:n.308+1158G>A