Canonical Allele Identifier: CA10652575
Gene: OPA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45550302C>T , CM000681.2:g.45550302C>T GRCh38
NC_000019.9:g.46053560C>T , CM000681.1:g.46053560C>T GRCh37
NC_000019.8:g.50745400C>T NCBI36
NG_013332.1:g.39563G>A

Transcript Alleles

HGVS Amino-acid Change
NM_025136.4:c.*3212G>A MANE Select NP_079412.1:n.*3212G>A
ENST00000263275.5:c.*3212G>A MANE Select ENSP00000263275.4:n.*3212G>A
NM_001017989.2:c.143-20846G>A NP_001017989.2:n.143-20846G>A
NM_001017989.3:c.143-20846G>A NP_001017989.2:n.143-20846G>A
NM_025136.3:c.*3212G>A NP_079412.1:n.*3212G>A
ENST00000263275.4:c.*3212G>A ENSP00000263275.3:n.*3212G>A
ENST00000323060.3:c.143-20846G>A ENSP00000319817.3:n.143-20846G>A
ENST00000323060.4:c.143-20846G>A ENSP00000319817.3:n.143-20846G>A
XM_006723403.4:c.*3212G>A XP_006723466.1:n.*3212G>A
XM_011527348.1:c.-17-20846G>A XP_011525650.1:n.-17-20846G>A