Canonical Allele Identifier: CA1925602661

Gene: OPN4

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86654812C= , CM000672.2:g.86654812C=	GRCh38
NC_000010.10:g.88414569C= , CM000672.1:g.88414569C=	GRCh37
NC_000010.9:g.88404549C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372071.7:c.29C=	ENSP00000361141.2:p.Pro10=
ENST00000443292.2:c.29C=	ENSP00000393132.2:p.Pro10=
ENST00000685347.1:n.145+150C=
ENST00000690949.1:n.145+150C=
ENST00000241891.10:c.29C= MANE Select	ENSP00000241891.5:p.Pro10=
ENST00000241891.9:c.29C=	ENSP00000241891.5:p.Pro10=
ENST00000372071.6:c.29C=	ENSP00000361141.2:p.Pro10=
ENST00000443292.1:c.29C=	ENSP00000393132.1:p.Pro10=
NM_001030015.2:c.29C=	NP_001025186.1:p.Pro10=
NM_033282.3:c.29C=	NP_150598.1:p.Pro10=
XM_017016955.1:c.29C=	XP_016872444.1:p.Pro10=
XM_017016956.1:c.29C=	XP_016872445.1:p.Pro10=
XM_017016957.1:c.-109+150C=	XP_016872446.1:n.-109+150C=
NM_033282.4:c.29C= MANE Select	NP_150598.1:p.Pro10=
NM_001030015.3:c.29C=	NP_001025186.1:p.Pro10=