Canonical Allele Identifier: CA308953783
Community Standard Title: NM_025136.4(OPA3):c.*6101A>G
Gene: OPA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45547413T>C , CM000681.2:g.45547413T>C GRCh38
NC_000019.9:g.46050671T>C , CM000681.1:g.46050671T>C GRCh37
NC_000019.8:g.50742511T>C NCBI36
NG_013332.1:g.42452A>G

Transcript Alleles

HGVS Amino-acid Change
NM_025136.4:c.*6101A>G MANE Select NP_079412.1:n.*6101A>G
ENST00000263275.5:c.*6101A>G MANE Select ENSP00000263275.4:n.*6101A>G
NM_001017989.2:c.143-17957A>G NP_001017989.2:n.143-17957A>G
NM_001017989.3:c.143-17957A>G NP_001017989.2:n.143-17957A>G
NM_025136.3:c.*6101A>G NP_079412.1:n.*6101A>G
ENST00000263275.4:c.*6101A>G ENSP00000263275.3:n.*6101A>G
ENST00000323060.3:c.143-17957A>G ENSP00000319817.3:n.143-17957A>G
ENST00000323060.4:c.143-17957A>G ENSP00000319817.3:n.143-17957A>G
XM_011527348.1:c.-17-17957A>G XP_011525650.1:n.-17-17957A>G