Canonical Allele Identifier: CA1173563408
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68444605C= , CM000663.2:g.68444605C= GRCh38
NC_000001.10:g.68910288C= , CM000663.1:g.68910288C= GRCh37
NC_000001.9:g.68682876C= NCBI36
NG_008472.1:g.10355G=
NG_008472.2:g.10355G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.421G= MANE Select ENSP00000262340.5:p.Glu141=
ENST00000262340.5:c.421G= ENSP00000262340.5:p.Glu141=
NM_000329.2:c.421G= NP_000320.1:p.Glu141=
XM_017002027.1:c.145G= XP_016857516.1:p.Glu49=
NM_000329.3:c.421G= MANE Select NP_000320.1:p.Glu141=