Canonical Allele Identifier: CA7200537

Gene: OTX2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.56804235G>T , CM000676.2:g.56804235G>T	GRCh38
NC_000014.8:g.57270953G>T , CM000676.1:g.57270953G>T	GRCh37
NC_000014.7:g.56340706G>T	NCBI36
NG_008204.1:g.11232C>A
NG_008204.2:g.17459C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_021728.4:c.226C>A MANE Select	NP_068374.1:p.Arg76=
ENST00000672264.2:c.226C>A MANE Select	ENSP00000500115.1:p.Arg76=
NM_001270523.1:c.202C>A	NP_001257452.1:p.Arg68=
NM_001270523.2:c.202C>A	NP_001257452.1:p.Arg68=
NM_001270524.1:c.202C>A	NP_001257453.1:p.Arg68=
NM_001270524.2:c.202C>A	NP_001257453.1:p.Arg68=
NM_001270525.1:c.226C>A	NP_001257454.1:p.Arg76=
NM_001270525.2:c.226C>A	NP_001257454.1:p.Arg76=
NM_021728.3:c.226C>A	NP_068374.1:p.Arg76=
NM_172337.2:c.202C>A	NP_758840.1:p.Arg68=
NM_172337.3:c.202C>A	NP_758840.1:p.Arg68=
NR_073034.1:n.381+1125C>A
NR_073034.2:n.384+1125C>A
NR_073036.1:n.304+1125C>A
NR_073036.2:n.308+1125C>A
ENST00000339475.10:c.202C>A	ENSP00000343819.5:p.Arg68=
ENST00000339475.9:c.226C>A	ENSP00000343819.4:p.Arg76=
ENST00000408990.7:c.202C>A	ENSP00000386185.3:p.Arg68=
ENST00000408990.8:c.202C>A	ENSP00000386185.3:p.Arg68=
ENST00000554559.5:c.97+1125C>A	ENSP00000450468.1:n.97+1125C>A
ENST00000554788.5:c.97+1125C>A	ENSP00000474486.1:n.97+1125C>A
ENST00000554845.1:c.226C>A	ENSP00000451357.1:p.Arg76=
ENST00000554845.2:c.226C>A	ENSP00000451357.2:p.Arg76=
ENST00000555006.5:c.202C>A	ENSP00000452336.1:p.Arg68=
ENST00000555804.1:c.202C>A	ENSP00000451272.1:p.Arg68=
ENST00000555804.2:c.202C>A	ENSP00000451272.2:p.Arg68=
ENST00000672125.1:c.202C>A	ENSP00000500744.1:p.Arg68=
ENST00000673035.1:c.202C>A	ENSP00000500061.1:p.Arg68=
ENST00000673481.1:c.226C>A	ENSP00000500595.1:p.Arg76=
ENST00000685244.1:c.202C>A	ENSP00000508798.1:p.Arg68=