Canonical Allele Identifier: CA2338489875
Gene: OPA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45553912C= , CM000681.2:g.45553912C= GRCh38
NC_000019.9:g.46057170C= , CM000681.1:g.46057170C= GRCh37
NC_000019.8:g.50749010C= NCBI36
NG_013332.1:g.35953G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323060.4:c.143-24456G= ENSP00000319817.3:n.143-24456G=
ENST00000263275.5:c.143-1G= MANE Select ENSP00000263275.4:n.143-1G=
ENST00000263275.4:c.143-1G= ENSP00000263275.3:n.143-1G=
ENST00000323060.3:c.143-24456G= ENSP00000319817.3:n.143-24456G=
ENST00000544371.1:c.-17-1G= ENSP00000442839.1:n.-17-1G=
NM_001017989.2:c.143-24456G= NP_001017989.2:n.143-24456G=
NM_025136.3:c.143-1G= NP_079412.1:n.143-1G=
XM_005259278.2:c.-17-1G= XP_005259335.1:n.-17-1G=
XM_006723403.2:c.-17-1G= XP_006723466.1:n.-17-1G=
XM_011527348.1:c.-17-24456G= XP_011525650.1:n.-17-24456G=
XM_006723403.4:c.-17-1G= XP_006723466.1:n.-17-1G=
NM_001017989.3:c.143-24456G= NP_001017989.2:n.143-24456G=
NM_025136.4:c.143-1G= MANE Select NP_079412.1:n.143-1G=