Canonical Allele Identifier: CA2010382187

Gene: OPCML

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.133251042C= , CM000673.2:g.133251042C=	GRCh38
NC_000011.9:g.133120937C= , CM000673.1:g.133120937C=	GRCh37
NC_000011.8:g.132626147C=	NCBI36
NG_012107.1:g.286467G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001012393.5:c.61+281222G= MANE Select	NP_001012393.1:n.61+281222G=
ENST00000524381.6:c.61+281222G= MANE Select	ENSP00000434750.1:n.61+281222G=
NM_001012393.1:c.61+281222G=	NP_001012393.1:n.61+281222G=
NM_001012393.2:c.61+281222G=	NP_001012393.1:n.61+281222G=
NM_001012393.3:c.61+281222G=	NP_001012393.1:n.61+281222G=
NM_001319104.1:c.-134+281222G=	NP_001306033.1:n.-134+281222G=
NM_001319104.2:c.-134+281222G=	NP_001306033.1:n.-134+281222G=
NM_001319104.4:c.-134+281222G=	NP_001306033.1:n.-134+281222G=
ENST00000524381.5:c.61+281222G=	ENSP00000434750.1:n.61+281222G=
ENST00000529038.5:n.139+281222G=
XM_006718846.1:c.61+281222G=	XP_006718909.1:n.61+281222G=
XM_006718846.3:c.61+281222G=	XP_006718909.1:n.61+281222G=
XM_011542856.1:c.-42+45982G=	XP_011541158.1:n.-42+45982G=
XM_011542856.3:c.-42+45982G=	XP_011541158.1:n.-42+45982G=
XR_429015.2:n.216-278G=