Canonical Allele Identifier: CA2139134215
Gene: OTX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.56801989T= , CM000676.2:g.56801989T= GRCh38
NC_000014.8:g.57268707T= , CM000676.1:g.57268707T= GRCh37
NC_000014.7:g.56338460T= NCBI36
NG_008204.1:g.13478A=
NG_008204.2:g.19705A=

Transcript Alleles

HGVS Amino-acid change
ENST00000554845.2:c.640A= ENSP00000451357.2:p.Thr214=
ENST00000555804.2:c.616A= ENSP00000451272.2:p.Thr206=
ENST00000685244.1:c.616A= ENSP00000508798.1:p.Thr206=
ENST00000339475.10:c.616A= ENSP00000343819.5:p.Thr206=
ENST00000408990.8:c.616A= ENSP00000386185.3:p.Thr206=
ENST00000672125.1:c.361-108A= ENSP00000500744.1:n.361-108A=
ENST00000672264.2:c.640A= MANE Select ENSP00000500115.1:p.Thr214=
ENST00000673035.1:c.616A= ENSP00000500061.1:p.Thr206=
ENST00000673481.1:c.640A= ENSP00000500595.1:p.Thr214=
ENST00000339475.9:c.640A= ENSP00000343819.4:p.Thr214=
ENST00000408990.7:c.616A= ENSP00000386185.3:p.Thr206=
ENST00000554788.5:c.*356A= ENSP00000474486.1:n.*356A=
ENST00000554845.1:c.640A= ENSP00000451357.1:p.Thr214=
ENST00000555006.5:c.616A= ENSP00000452336.1:p.Thr206=
NM_001270523.1:c.616A= NP_001257452.1:p.Thr206=
NM_001270524.1:c.616A= NP_001257453.1:p.Thr206=
NM_001270525.1:c.640A= NP_001257454.1:p.Thr214=
NM_021728.3:c.640A= NP_068374.1:p.Thr214=
NM_172337.2:c.616A= NP_758840.1:p.Thr206=
NR_073034.1:n.748A=
NR_073036.1:n.671A=
NM_001270523.2:c.616A= NP_001257452.1:p.Thr206=
NM_001270524.2:c.616A= NP_001257453.1:p.Thr206=
NM_001270525.2:c.640A= NP_001257454.1:p.Thr214=
NM_021728.4:c.640A= MANE Select NP_068374.1:p.Thr214=
NM_172337.3:c.616A= NP_758840.1:p.Thr206=
NR_073034.2:n.751A=
NR_073036.2:n.675A=