Canonical Allele Identifier: CA486669099

Gene: OTX2

Linked Data

• MyVariant Identifiers: chr14:g.57268960C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.56802242C>G , CM000676.2:g.56802242C>G	GRCh38
NC_000014.8:g.57268960C>G , CM000676.1:g.57268960C>G	GRCh37
NC_000014.7:g.56338713C>G	NCBI36
NG_008204.1:g.13225G>C
NG_008204.2:g.19452G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000554845.2:c.387G>C	ENSP00000451357.2:p.Val129=
ENST00000555804.2:c.363G>C	ENSP00000451272.2:p.Val121=
ENST00000685244.1:c.363G>C	ENSP00000508798.1:p.Val121=
ENST00000339475.10:c.363G>C	ENSP00000343819.5:p.Val121=
ENST00000408990.8:c.363G>C	ENSP00000386185.3:p.Val121=
ENST00000672125.1:c.360+3G>C	ENSP00000500744.1:n.360+3G>C
ENST00000672264.2:c.387G>C MANE Select	ENSP00000500115.1:p.Val129=
ENST00000673035.1:c.363G>C	ENSP00000500061.1:p.Val121=
ENST00000673481.1:c.387G>C	ENSP00000500595.1:p.Val129=
ENST00000339475.9:c.387G>C	ENSP00000343819.4:p.Val129=
ENST00000408990.7:c.363G>C	ENSP00000386185.3:p.Val121=
ENST00000554559.5:c.*103G>C	ENSP00000450468.1:n.*103G>C
ENST00000554788.5:c.*103G>C	ENSP00000474486.1:n.*103G>C
ENST00000554845.1:c.387G>C	ENSP00000451357.1:p.Val129=
ENST00000555006.5:c.363G>C	ENSP00000452336.1:p.Val121=
ENST00000555804.1:c.363G>C	ENSP00000451272.1:p.Val121=
NM_001270523.1:c.363G>C	NP_001257452.1:p.Val121=
NM_001270524.1:c.363G>C	NP_001257453.1:p.Val121=
NM_001270525.1:c.387G>C	NP_001257454.1:p.Val129=
NM_021728.3:c.387G>C	NP_068374.1:p.Val129=
NM_172337.2:c.363G>C	NP_758840.1:p.Val121=
NR_073034.1:n.495G>C
NR_073036.1:n.418G>C
NM_001270523.2:c.363G>C	NP_001257452.1:p.Val121=
NM_001270524.2:c.363G>C	NP_001257453.1:p.Val121=
NM_001270525.2:c.387G>C	NP_001257454.1:p.Val129=
NM_021728.4:c.387G>C MANE Select	NP_068374.1:p.Val129=
NM_172337.3:c.363G>C	NP_758840.1:p.Val121=
NR_073034.2:n.498G>C
NR_073036.2:n.422G>C