Canonical Allele Identifier: CA437434345

Gene: OPA1

Linked Data

• MyVariant Identifiers: chr3:g.193355752T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.193637963T>C , CM000665.2:g.193637963T>C	GRCh38
NC_000003.11:g.193355752T>C , CM000665.1:g.193355752T>C	GRCh37
NC_000003.10:g.194838446T>C	NCBI36
NG_011605.1:g.49820T>C , LRG_337:g.49820T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000361510.8:c.1047T>C MANE Select	ENSP00000355324.2:p.Val349=
ENST00000361828.7:c.882T>C	ENSP00000354429.3:p.Val294=
ENST00000361908.8:c.993T>C	ENSP00000354681.3:p.Val331=
ENST00000392436.7:c.882T>C	ENSP00000376231.3:p.Val294=
ENST00000392437.6:c.936T>C	ENSP00000376232.2:p.Val312=
ENST00000642289.1:c.977T>C
ENST00000642445.1:c.882T>C	ENSP00000495535.1:p.Val294=
ENST00000642593.1:c.882T>C	ENSP00000494273.1:p.Val294=
ENST00000643329.1:c.564T>C	ENSP00000493673.1:p.Val188=
ENST00000643737.1:c.*963T>C	ENSP00000494210.1:n.*963T>C
ENST00000644595.1:c.882T>C	ENSP00000494121.1:p.Val294=
ENST00000644629.1:c.542T>C
ENST00000644841.1:c.510T>C	ENSP00000493988.1:p.Val170=
ENST00000644959.1:c.851T>C
ENST00000645553.1:c.897T>C	ENSP00000494725.1:p.Val299=
ENST00000646085.1:c.*360T>C	ENSP00000494509.1:n.*360T>C
ENST00000646277.1:c.1047T>C	ENSP00000495289.1:p.Val349=
ENST00000646699.1:c.977T>C
ENST00000646793.1:c.774T>C	ENSP00000494512.1:p.Val258=
ENST00000361150.6:c.885T>C	ENSP00000354781.2:p.Val295=
ENST00000361510.6:c.1047T>C	ENSP00000355324.2:p.Val349=
ENST00000361715.6:c.939T>C	ENSP00000355311.2:p.Val313=
ENST00000361828.6:c.936T>C	ENSP00000354429.2:p.Val312=
ENST00000361908.7:c.993T>C	ENSP00000354681.3:p.Val331=
ENST00000392438.7:c.882T>C	ENSP00000376233.3:p.Val294=
ENST00000475899.1:n.78T>C
ENST00000495476.1:n.403T>C
ENST00000497189.5:n.368T>C
NM_015560.2:c.882T>C , LRG_337t1:c.882T>C	NP_056375.2:p.Val294=
NM_130831.2:c.774T>C	NP_570844.1:p.Val258=
NM_130832.2:c.828T>C	NP_570845.1:p.Val276=
NM_130833.2:c.885T>C	NP_570846.1:p.Val295=
NM_130834.2:c.936T>C	NP_570847.2:p.Val312=
NM_130835.2:c.939T>C	NP_570848.1:p.Val313=
NM_130836.2:c.993T>C	NP_570849.2:p.Val331=
NM_130837.2:c.1047T>C , LRG_337t2:c.1047T>C	NP_570850.2:p.Val349=
XM_011512863.1:c.1047T>C	XP_011511165.1:p.Val349=
XM_011512864.1:c.993T>C	XP_011511166.1:p.Val331=
XM_011512865.1:c.936T>C	XP_011511167.1:p.Val312=
XM_011512866.1:c.885T>C	XP_011511168.1:p.Val295=
XM_011512867.1:c.882T>C	XP_011511169.1:p.Val294=
XM_011512868.1:c.774T>C	XP_011511170.1:p.Val258=
XM_011512869.1:c.1047T>C	XP_011511171.1:p.Val349=
NM_001354663.1:c.513T>C	NP_001341592.1:p.Val171=
NM_001354664.1:c.510T>C	NP_001341593.1:p.Val170=
XR_001740158.2:n.1276T>C
XR_001740159.2:n.1111T>C
NM_001354663.2:c.513T>C	NP_001341592.1:p.Val171=
NM_001354664.2:c.510T>C	NP_001341593.1:p.Val170=
NM_130831.3:c.774T>C	NP_570844.1:p.Val258=
NM_130832.3:c.828T>C	NP_570845.1:p.Val276=
NM_130834.3:c.936T>C	NP_570847.2:p.Val312=
NM_130836.3:c.993T>C	NP_570849.2:p.Val331=
NM_015560.3:c.882T>C	NP_056375.2:p.Val294=
NM_130833.3:c.885T>C	NP_570846.1:p.Val295=
NM_130835.3:c.939T>C	NP_570848.1:p.Val313=
NM_130837.3:c.1047T>C MANE Select	NP_570850.2:p.Val349=