Canonical Allele Identifier: CA1173557934
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431148_68431149delinsTC , CM000663.2:g.68431148_68431149delinsTC GRCh38
NC_000001.10:g.68896831_68896832delinsTC , CM000663.1:g.68896831_68896832delinsTC GRCh37
NC_000001.9:g.68669419_68669420delinsTC NCBI36
NG_008472.1:g.23811_23812delinsGA
NG_008472.2:g.23811_23812delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1366_1367delinsGA MANE Select ENSP00000262340.5:p.Glu456=
ENST00000262340.5:c.1366_1367delinsGA ENSP00000262340.5:p.Glu456=
NM_000329.2:c.1366_1367delinsGA NP_000320.1:p.Glu456=
XM_017002027.1:c.1090_1091delinsGA XP_016857516.1:p.Glu364=
NM_000329.3:c.1366_1367delinsGA MANE Select NP_000320.1:p.Glu456=