Canonical Allele Identifier: CA1140725789
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68444582C= , CM000663.2:g.68444582C= GRCh38
NC_000001.10:g.68910265C= , CM000663.1:g.68910265C= GRCh37
NC_000001.9:g.68682853C= NCBI36
NG_008472.1:g.10378G=
NG_008472.2:g.10378G=

Transcript Alleles

HGVS Amino-acid change
ENST00000262340.6:c.444G= MANE Select ENSP00000262340.5:p.Glu148=
ENST00000262340.5:c.444G= ENSP00000262340.5:p.Glu148=
NM_000329.2:c.444G= NP_000320.1:p.Glu148=
XM_017002027.1:c.168G= XP_016857516.1:p.Glu56=
NM_000329.3:c.444G= MANE Select NP_000320.1:p.Glu148=