Canonical Allele Identifier: CA390052209
Community Standard Title: NM_021728.4(OTX2):c.278G>A (p.Trp93Ter)
Gene: OTX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.56802351C>T , CM000676.2:g.56802351C>T GRCh38
NC_000014.8:g.57269069C>T , CM000676.1:g.57269069C>T GRCh37
NC_000014.7:g.56338822C>T NCBI36
NG_008204.1:g.13116G>A
NG_008204.2:g.19343G>A

Transcript Alleles

HGVS Amino-acid Change
NM_021728.4:c.278G>A MANE Select NP_068374.1:p.Trp93Ter
ENST00000672264.2:c.278G>A MANE Select ENSP00000500115.1:p.Trp93Ter
NM_001270523.1:c.254G>A NP_001257452.1:p.Trp85Ter
NM_001270523.2:c.254G>A NP_001257452.1:p.Trp85Ter
NM_001270524.1:c.254G>A NP_001257453.1:p.Trp85Ter
NM_001270524.2:c.254G>A NP_001257453.1:p.Trp85Ter
NM_001270525.1:c.278G>A NP_001257454.1:p.Trp93Ter
NM_001270525.2:c.278G>A NP_001257454.1:p.Trp93Ter
NM_021728.3:c.278G>A NP_068374.1:p.Trp93Ter
NM_172337.2:c.254G>A NP_758840.1:p.Trp85Ter
NM_172337.3:c.254G>A NP_758840.1:p.Trp85Ter
NR_073034.1:n.386G>A
NR_073034.2:n.389G>A
NR_073036.1:n.309G>A
NR_073036.2:n.313G>A
ENST00000339475.10:c.254G>A ENSP00000343819.5:p.Trp85Ter
ENST00000339475.9:c.278G>A ENSP00000343819.4:p.Trp93Ter
ENST00000408990.7:c.254G>A ENSP00000386185.3:p.Trp85Ter
ENST00000408990.8:c.254G>A ENSP00000386185.3:p.Trp85Ter
ENST00000554559.5:c.102G>A ENSP00000450468.1:p.Met34Ile
ENST00000554788.5:c.102G>A ENSP00000474486.1:p.Met34Ile
ENST00000554845.1:c.278G>A ENSP00000451357.1:p.Trp93Ter
ENST00000554845.2:c.278G>A ENSP00000451357.2:p.Trp93Ter
ENST00000555006.5:c.254G>A ENSP00000452336.1:p.Trp85Ter
ENST00000555804.1:c.254G>A ENSP00000451272.1:p.Trp85Ter
ENST00000555804.2:c.254G>A ENSP00000451272.2:p.Trp85Ter
ENST00000672125.1:c.254G>A ENSP00000500744.1:p.Trp85Ter
ENST00000673035.1:c.254G>A ENSP00000500061.1:p.Trp85Ter
ENST00000673481.1:c.278G>A ENSP00000500595.1:p.Trp93Ter
ENST00000685244.1:c.254G>A ENSP00000508798.1:p.Trp85Ter