Canonical Allele Identifier: CA1140762632
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431145G= , CM000663.2:g.68431145G= GRCh38
NC_000001.10:g.68896828G= , CM000663.1:g.68896828G= GRCh37
NC_000001.9:g.68669416G= NCBI36
NG_008472.1:g.23815C=
NG_008472.2:g.23815C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1370C= MANE Select ENSP00000262340.5:p.Thr457=
ENST00000262340.5:c.1370C= ENSP00000262340.5:p.Thr457=
NM_000329.2:c.1370C= NP_000320.1:p.Thr457=
XM_017002027.1:c.1094C= XP_016857516.1:p.Thr365=
NM_000329.3:c.1370C= MANE Select NP_000320.1:p.Thr457=