Canonical Allele Identifier: CA390051259

Gene: OTX2

Linked Data

• MyVariant Identifiers: chr14:g.57268625T>C (hg19) ; chr14:g.56801907T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.56801907T>C , CM000676.2:g.56801907T>C	GRCh38
NC_000014.8:g.57268625T>C , CM000676.1:g.57268625T>C	GRCh37
NC_000014.7:g.56338378T>C	NCBI36
NG_008204.1:g.13560A>G
NG_008204.2:g.19787A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000554845.2:c.722A>G	ENSP00000451357.2:p.Gln241Arg
ENST00000555804.2:c.698A>G	ENSP00000451272.2:p.Gln233Arg
ENST00000685244.1:c.698A>G	ENSP00000508798.1:p.Gln233Arg
ENST00000339475.10:c.698A>G	ENSP00000343819.5:p.Gln233Arg
ENST00000408990.8:c.698A>G	ENSP00000386185.3:p.Gln233Arg
ENST00000672125.1:c.361-26A>G	ENSP00000500744.1:n.361-26A>G
ENST00000672264.2:c.722A>G MANE Select	ENSP00000500115.1:p.Gln241Arg
ENST00000673035.1:c.698A>G	ENSP00000500061.1:p.Gln233Arg
ENST00000673481.1:c.722A>G	ENSP00000500595.1:p.Gln241Arg
ENST00000339475.9:c.722A>G	ENSP00000343819.4:p.Gln241Arg
ENST00000408990.7:c.698A>G	ENSP00000386185.3:p.Gln233Arg
ENST00000554788.5:c.*438A>G	ENSP00000474486.1:n.*438A>G
ENST00000555006.5:c.698A>G	ENSP00000452336.1:p.Gln233Arg
NM_001270523.1:c.698A>G	NP_001257452.1:p.Gln233Arg
NM_001270524.1:c.698A>G	NP_001257453.1:p.Gln233Arg
NM_001270525.1:c.722A>G	NP_001257454.1:p.Gln241Arg
NM_021728.3:c.722A>G	NP_068374.1:p.Gln241Arg
NM_172337.2:c.698A>G	NP_758840.1:p.Gln233Arg
NR_073034.1:n.830A>G
NR_073036.1:n.753A>G
NM_001270523.2:c.698A>G	NP_001257452.1:p.Gln233Arg
NM_001270524.2:c.698A>G	NP_001257453.1:p.Gln233Arg
NM_001270525.2:c.722A>G	NP_001257454.1:p.Gln241Arg
NM_021728.4:c.722A>G MANE Select	NP_068374.1:p.Gln241Arg
NM_172337.3:c.698A>G	NP_758840.1:p.Gln233Arg
NR_073034.2:n.833A>G
NR_073036.2:n.757A>G