Canonical Allele Identifier: CA377440823

Gene: OPN4

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372071.7:c.29C>G	ENSP00000361141.2:p.Pro10Arg
ENST00000443292.2:c.29C>G	ENSP00000393132.2:p.Pro10Arg
ENST00000685347.1:n.145+150C>G
ENST00000690949.1:n.145+150C>G
ENST00000241891.10:c.29C>G MANE Select	ENSP00000241891.5:p.Pro10Arg
ENST00000241891.9:c.29C>G	ENSP00000241891.5:p.Pro10Arg
ENST00000372071.6:c.29C>G	ENSP00000361141.2:p.Pro10Arg
ENST00000443292.1:c.29C>G	ENSP00000393132.1:p.Pro10Arg
NM_001030015.2:c.29C>G	NP_001025186.1:p.Pro10Arg
NM_033282.3:c.29C>G	NP_150598.1:p.Pro10Arg
XM_017016955.1:c.29C>G	XP_016872444.1:p.Pro10Arg
XM_017016956.1:c.29C>G	XP_016872445.1:p.Pro10Arg
XM_017016957.1:c.-109+150C>G	XP_016872446.1:n.-109+150C>G
NM_033282.4:c.29C>G MANE Select	NP_150598.1:p.Pro10Arg
NM_001030015.3:c.29C>G	NP_001025186.1:p.Pro10Arg