Canonical Allele Identifier: CA2759720

Gene: OPA1

Linked Data

• dbSNP Id: rs757223742
• ExAC: 3:193380778 A / C
• gnomAD v2: 3-193380778-A-C
• MyVariant Identifiers: chr3:g.193380778A>C (hg19) ; chr3:g.193662989A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193662989A>C , CM000665.2:g.193662989A>C	GRCh38
NC_000003.11:g.193380778A>C , CM000665.1:g.193380778A>C	GRCh37
NC_000003.10:g.194863472A>C	NCBI36
NG_011605.1:g.74846A>C , LRG_337:g.74846A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361510.8:c.2661+27A>C MANE Select	ENSP00000355324.2:n.2661+27A>C
ENST00000361828.7:c.2496+27A>C	ENSP00000354429.3:n.2496+27A>C
ENST00000361908.8:c.2607+27A>C	ENSP00000354681.3:n.2607+27A>C
ENST00000392436.7:c.2496+27A>C	ENSP00000376231.3:n.2496+27A>C
ENST00000392437.6:c.2550+27A>C	ENSP00000376232.2:n.2550+27A>C
ENST00000642289.1:c.2435+27A>C
ENST00000642445.1:c.2496+27A>C	ENSP00000495535.1:n.2496+27A>C
ENST00000642593.1:c.*721+27A>C	ENSP00000494273.1:n.*721+27A>C
ENST00000643329.1:c.2178+27A>C	ENSP00000493673.1:n.2178+27A>C
ENST00000643737.1:c.*2577+27A>C	ENSP00000494210.1:n.*2577+27A>C
ENST00000644595.1:c.2496+27A>C	ENSP00000494121.1:n.2496+27A>C
ENST00000644629.1:c.2083+27A>C
ENST00000644841.1:c.*980+27A>C	ENSP00000493988.1:n.*980+27A>C
ENST00000644959.1:c.2490+27A>C
ENST00000645553.1:c.2511+27A>C	ENSP00000494725.1:n.2511+27A>C
ENST00000646085.1:c.*1974+27A>C	ENSP00000494509.1:n.*1974+27A>C
ENST00000646277.1:c.*1097+27A>C	ENSP00000495289.1:n.*1097+27A>C
ENST00000646544.1:c.1484+27A>C
ENST00000646699.1:c.2435+27A>C
ENST00000646793.1:c.2388+27A>C	ENSP00000494512.1:n.2388+27A>C
ENST00000361150.6:c.2499+27A>C	ENSP00000354781.2:n.2499+27A>C
ENST00000361510.6:c.2661+27A>C	ENSP00000355324.2:n.2661+27A>C
ENST00000361715.6:c.2553+27A>C	ENSP00000355311.2:n.2553+27A>C
ENST00000361828.6:c.2550+27A>C	ENSP00000354429.2:n.2550+27A>C
ENST00000361908.7:c.2607+27A>C	ENSP00000354681.3:n.2607+27A>C
ENST00000392438.7:c.2496+27A>C	ENSP00000376233.3:n.2496+27A>C
ENST00000445863.1:c.72+27A>C	ENSP00000398358.1:n.72+27A>C
NM_015560.2:c.2496+27A>C , LRG_337t1:c.2496+27A>C	NP_056375.2:n.2496+27A>C
NM_130831.2:c.2388+27A>C	NP_570844.1:n.2388+27A>C
NM_130832.2:c.2442+27A>C	NP_570845.1:n.2442+27A>C
NM_130833.2:c.2499+27A>C	NP_570846.1:n.2499+27A>C
NM_130834.2:c.2550+27A>C	NP_570847.2:n.2550+27A>C
NM_130835.2:c.2553+27A>C	NP_570848.1:n.2553+27A>C
NM_130836.2:c.2607+27A>C	NP_570849.2:n.2607+27A>C
NM_130837.2:c.2661+27A>C , LRG_337t2:c.2661+27A>C	NP_570850.2:n.2661+27A>C
XM_011512863.1:c.2661+27A>C	XP_011511165.1:n.2661+27A>C
XM_011512864.1:c.2607+27A>C	XP_011511166.1:n.2607+27A>C
XM_011512865.1:c.2550+27A>C	XP_011511167.1:n.2550+27A>C
XM_011512866.1:c.2499+27A>C	XP_011511168.1:n.2499+27A>C
XM_011512867.1:c.2496+27A>C	XP_011511169.1:n.2496+27A>C
XM_011512868.1:c.2388+27A>C	XP_011511170.1:n.2388+27A>C
XR_924835.1:n.582+5931T>G
NM_001354663.1:c.2127+27A>C	NP_001341592.1:n.2127+27A>C
NM_001354664.1:c.2124+27A>C	NP_001341593.1:n.2124+27A>C
XR_001740158.2:n.2915+27A>C
XR_001740159.2:n.2750+27A>C
XR_001741072.1:n.601-2904T>G
XR_001741074.1:n.475+7819T>G
XR_924835.2:n.600+5931T>G
NM_001354663.2:c.2127+27A>C	NP_001341592.1:n.2127+27A>C
NM_001354664.2:c.2124+27A>C	NP_001341593.1:n.2124+27A>C
NM_130831.3:c.2388+27A>C	NP_570844.1:n.2388+27A>C
NM_130832.3:c.2442+27A>C	NP_570845.1:n.2442+27A>C
NM_130834.3:c.2550+27A>C	NP_570847.2:n.2550+27A>C
NM_130836.3:c.2607+27A>C	NP_570849.2:n.2607+27A>C
NM_015560.3:c.2496+27A>C	NP_056375.2:n.2496+27A>C
NM_130833.3:c.2499+27A>C	NP_570846.1:n.2499+27A>C
NM_130835.3:c.2553+27A>C	NP_570848.1:n.2553+27A>C
NM_130837.3:c.2661+27A>C MANE Select	NP_570850.2:n.2661+27A>C