Canonical Allele Identifier: CA376029109
Gene: OPTN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.13124083A>G , CM000672.2:g.13124083A>G GRCh38
NC_000010.10:g.13166083A>G , CM000672.1:g.13166083A>G GRCh37
NC_000010.9:g.13206089A>G NCBI36
NG_012876.1:g.29002A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378747.8:c.971A>G MANE Select ENSP00000368021.3:p.Glu324Gly
ENST00000263036.9:c.971A>G ENSP00000263036.3:p.Glu324Gly
ENST00000378747.7:c.971A>G ENSP00000368021.3:p.Glu324Gly
ENST00000378748.7:c.971A>G ENSP00000368022.3:p.Glu324Gly
ENST00000378752.7:c.953A>G ENSP00000368027.3:p.Glu318Gly
ENST00000378757.6:c.971A>G ENSP00000368032.2:p.Glu324Gly
ENST00000378764.6:c.953A>G ENSP00000368040.1:p.Glu318Gly
NM_001008211.1:c.971A>G NP_001008212.1:p.Glu324Gly
NM_001008212.1:c.971A>G NP_001008213.1:p.Glu324Gly
NM_001008213.1:c.971A>G NP_001008214.1:p.Glu324Gly
NM_021980.4:c.971A>G NP_068815.2:p.Glu324Gly
XM_005252336.2:c.953A>G XP_005252393.2:p.Glu318Gly
XM_005252337.3:c.953A>G XP_005252394.2:p.Glu318Gly
XM_005252338.2:c.800A>G XP_005252395.2:p.Glu267Gly
NM_001008212.2:c.971A>G MANE Select NP_001008213.1:p.Glu324Gly