Canonical Allele Identifier: CA355788173

Gene: OPA1

Linked Data

• ClinVar Variation Id: 802038
• ClinVar RCV Id: RCV000987378 ; RCV001374996
• dbSNP Id: rs1577228080
• MyVariant Identifiers: chr3:g.193355756G>C (hg19) ; chr3:g.193637967G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193637967G>C , CM000665.2:g.193637967G>C	GRCh38
NC_000003.11:g.193355756G>C , CM000665.1:g.193355756G>C	GRCh37
NC_000003.10:g.194838450G>C	NCBI36
NG_011605.1:g.49824G>C , LRG_337:g.49824G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000361510.8:c.1051G>C MANE Select	ENSP00000355324.2:p.Asp351His
ENST00000361828.7:c.886G>C	ENSP00000354429.3:p.Asp296His
ENST00000361908.8:c.997G>C	ENSP00000354681.3:p.Asp333His
ENST00000392436.7:c.886G>C	ENSP00000376231.3:p.Asp296His
ENST00000392437.6:c.940G>C	ENSP00000376232.2:p.Asp314His
ENST00000642289.1:c.981G>C
ENST00000642445.1:c.886G>C	ENSP00000495535.1:p.Asp296His
ENST00000642593.1:c.886G>C	ENSP00000494273.1:p.Asp296His
ENST00000643329.1:c.568G>C	ENSP00000493673.1:p.Asp190His
ENST00000643737.1:c.*967G>C	ENSP00000494210.1:n.*967G>C
ENST00000644595.1:c.886G>C	ENSP00000494121.1:p.Asp296His
ENST00000644629.1:c.546G>C
ENST00000644841.1:c.514G>C	ENSP00000493988.1:p.Asp172His
ENST00000644959.1:c.855G>C
ENST00000645553.1:c.901G>C	ENSP00000494725.1:p.Asp301His
ENST00000646085.1:c.*364G>C	ENSP00000494509.1:n.*364G>C
ENST00000646277.1:c.1051G>C	ENSP00000495289.1:p.Asp351His
ENST00000646699.1:c.981G>C
ENST00000646793.1:c.778G>C	ENSP00000494512.1:p.Asp260His
ENST00000361150.6:c.889G>C	ENSP00000354781.2:p.Asp297His
ENST00000361510.6:c.1051G>C	ENSP00000355324.2:p.Asp351His
ENST00000361715.6:c.943G>C	ENSP00000355311.2:p.Asp315His
ENST00000361828.6:c.940G>C	ENSP00000354429.2:p.Asp314His
ENST00000361908.7:c.997G>C	ENSP00000354681.3:p.Asp333His
ENST00000392438.7:c.886G>C	ENSP00000376233.3:p.Asp296His
ENST00000475899.1:n.82G>C
ENST00000495476.1:n.407G>C
ENST00000497189.5:n.372G>C
NM_015560.2:c.886G>C , LRG_337t1:c.886G>C	NP_056375.2:p.Asp296His
NM_130831.2:c.778G>C	NP_570844.1:p.Asp260His
NM_130832.2:c.832G>C	NP_570845.1:p.Asp278His
NM_130833.2:c.889G>C	NP_570846.1:p.Asp297His
NM_130834.2:c.940G>C	NP_570847.2:p.Asp314His
NM_130835.2:c.943G>C	NP_570848.1:p.Asp315His
NM_130836.2:c.997G>C	NP_570849.2:p.Asp333His
NM_130837.2:c.1051G>C , LRG_337t2:c.1051G>C	NP_570850.2:p.Asp351His
XM_011512863.1:c.1051G>C	XP_011511165.1:p.Asp351His
XM_011512864.1:c.997G>C	XP_011511166.1:p.Asp333His
XM_011512865.1:c.940G>C	XP_011511167.1:p.Asp314His
XM_011512866.1:c.889G>C	XP_011511168.1:p.Asp297His
XM_011512867.1:c.886G>C	XP_011511169.1:p.Asp296His
XM_011512868.1:c.778G>C	XP_011511170.1:p.Asp260His
XM_011512869.1:c.1051G>C	XP_011511171.1:p.Asp351His
NM_001354663.1:c.517G>C	NP_001341592.1:p.Asp173His
NM_001354664.1:c.514G>C	NP_001341593.1:p.Asp172His
XR_001740158.2:n.1280G>C
XR_001740159.2:n.1115G>C
NM_001354663.2:c.517G>C	NP_001341592.1:p.Asp173His
NM_001354664.2:c.514G>C	NP_001341593.1:p.Asp172His
NM_130831.3:c.778G>C	NP_570844.1:p.Asp260His
NM_130832.3:c.832G>C	NP_570845.1:p.Asp278His
NM_130834.3:c.940G>C	NP_570847.2:p.Asp314His
NM_130836.3:c.997G>C	NP_570849.2:p.Asp333His
NM_015560.3:c.886G>C	NP_056375.2:p.Asp296His
NM_130833.3:c.889G>C	NP_570846.1:p.Asp297His
NM_130835.3:c.943G>C	NP_570848.1:p.Asp315His
NM_130837.3:c.1051G>C MANE Select	NP_570850.2:p.Asp351His