Canonical Allele Identifier: CA10643006
Gene: OPA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45550618C>T , CM000681.2:g.45550618C>T GRCh38
NC_000019.9:g.46053876C>T , CM000681.1:g.46053876C>T GRCh37
NC_000019.8:g.50745716C>T NCBI36
NG_013332.1:g.39247G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000323060.4:c.143-21162G>A ENSP00000319817.3:n.143-21162G>A
ENST00000263275.5:c.*2896G>A MANE Select ENSP00000263275.4:n.*2896G>A
ENST00000263275.4:c.*2896G>A ENSP00000263275.3:n.*2896G>A
ENST00000323060.3:c.143-21162G>A ENSP00000319817.3:n.143-21162G>A
NM_001017989.2:c.143-21162G>A NP_001017989.2:n.143-21162G>A
NM_025136.3:c.*2896G>A NP_079412.1:n.*2896G>A
XM_011527348.1:c.-17-21162G>A XP_011525650.1:n.-17-21162G>A
XM_006723403.4:c.*2896G>A XP_006723466.1:n.*2896G>A
NM_001017989.3:c.143-21162G>A NP_001017989.2:n.143-21162G>A
NM_025136.4:c.*2896G>A MANE Select NP_079412.1:n.*2896G>A