Canonical Allele Identifier: CA355792814

Gene: OPA1

Linked Data

• MyVariant Identifiers: chr3:g.193377279G>C (hg19) ; chr3:g.193659490G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193659490G>C , CM000665.2:g.193659490G>C	GRCh38
NC_000003.11:g.193377279G>C , CM000665.1:g.193377279G>C	GRCh37
NC_000003.10:g.194859973G>C	NCBI36
NG_011605.1:g.71347G>C , LRG_337:g.71347G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361510.8:c.2449G>C MANE Select	ENSP00000355324.2:p.Ala817Pro
ENST00000361828.7:c.2284G>C	ENSP00000354429.3:p.Ala762Pro
ENST00000361908.8:c.2395G>C	ENSP00000354681.3:p.Ala799Pro
ENST00000392436.7:c.2284G>C	ENSP00000376231.3:p.Ala762Pro
ENST00000392437.6:c.2338G>C	ENSP00000376232.2:p.Ala780Pro
ENST00000642289.1:c.2223G>C
ENST00000642445.1:c.2284G>C	ENSP00000495535.1:p.Ala762Pro
ENST00000642593.1:c.*509G>C	ENSP00000494273.1:n.*509G>C
ENST00000643329.1:c.1966G>C	ENSP00000493673.1:p.Ala656Pro
ENST00000643737.1:c.*2365G>C	ENSP00000494210.1:n.*2365G>C
ENST00000644595.1:c.2284G>C	ENSP00000494121.1:p.Ala762Pro
ENST00000644629.1:c.1871G>C
ENST00000644841.1:c.*768G>C	ENSP00000493988.1:n.*768G>C
ENST00000644959.1:c.2278G>C
ENST00000645553.1:c.2299G>C	ENSP00000494725.1:p.Ala767Pro
ENST00000646085.1:c.*1762G>C	ENSP00000494509.1:n.*1762G>C
ENST00000646277.1:c.*885G>C	ENSP00000495289.1:n.*885G>C
ENST00000646544.1:c.1272G>C
ENST00000646699.1:c.2223G>C
ENST00000646793.1:c.2176G>C	ENSP00000494512.1:p.Ala726Pro
ENST00000361150.6:c.2287G>C	ENSP00000354781.2:p.Ala763Pro
ENST00000361510.6:c.2449G>C	ENSP00000355324.2:p.Ala817Pro
ENST00000361715.6:c.2341G>C	ENSP00000355311.2:p.Ala781Pro
ENST00000361828.6:c.2338G>C	ENSP00000354429.2:p.Ala780Pro
ENST00000361908.7:c.2395G>C	ENSP00000354681.3:p.Ala799Pro
ENST00000392438.7:c.2284G>C	ENSP00000376233.3:p.Ala762Pro
ENST00000482865.1:n.543G>C
NM_015560.2:c.2284G>C , LRG_337t1:c.2284G>C	NP_056375.2:p.Ala762Pro
NM_130831.2:c.2176G>C	NP_570844.1:p.Ala726Pro
NM_130832.2:c.2230G>C	NP_570845.1:p.Ala744Pro
NM_130833.2:c.2287G>C	NP_570846.1:p.Ala763Pro
NM_130834.2:c.2338G>C	NP_570847.2:p.Ala780Pro
NM_130835.2:c.2341G>C	NP_570848.1:p.Ala781Pro
NM_130836.2:c.2395G>C	NP_570849.2:p.Ala799Pro
NM_130837.2:c.2449G>C , LRG_337t2:c.2449G>C	NP_570850.2:p.Ala817Pro
XM_011512863.1:c.2449G>C	XP_011511165.1:p.Ala817Pro
XM_011512864.1:c.2395G>C	XP_011511166.1:p.Ala799Pro
XM_011512865.1:c.2338G>C	XP_011511167.1:p.Ala780Pro
XM_011512866.1:c.2287G>C	XP_011511168.1:p.Ala763Pro
XM_011512867.1:c.2284G>C	XP_011511169.1:p.Ala762Pro
XM_011512868.1:c.2176G>C	XP_011511170.1:p.Ala726Pro
XR_924835.1:n.582+9430C>G
NM_001354663.1:c.1915G>C	NP_001341592.1:p.Ala639Pro
NM_001354664.1:c.1912G>C	NP_001341593.1:p.Ala638Pro
XR_001740158.2:n.2703G>C
XR_001740159.2:n.2538G>C
XR_001741074.1:n.475+11318C>G
XR_924835.2:n.600+9430C>G
NM_001354663.2:c.1915G>C	NP_001341592.1:p.Ala639Pro
NM_001354664.2:c.1912G>C	NP_001341593.1:p.Ala638Pro
NM_130831.3:c.2176G>C	NP_570844.1:p.Ala726Pro
NM_130832.3:c.2230G>C	NP_570845.1:p.Ala744Pro
NM_130834.3:c.2338G>C	NP_570847.2:p.Ala780Pro
NM_130836.3:c.2395G>C	NP_570849.2:p.Ala799Pro
NM_015560.3:c.2284G>C	NP_056375.2:p.Ala762Pro
NM_130833.3:c.2287G>C	NP_570846.1:p.Ala763Pro
NM_130835.3:c.2341G>C	NP_570848.1:p.Ala781Pro
NM_130837.3:c.2449G>C MANE Select	NP_570850.2:p.Ala817Pro