Canonical Allele Identifier: CA1145145112
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431139A= , CM000663.2:g.68431139A= GRCh38
NC_000001.10:g.68896822A= , CM000663.1:g.68896822A= GRCh37
NC_000001.9:g.68669410A= NCBI36
NG_008472.1:g.23821T=
NG_008472.2:g.23821T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1376T= MANE Select ENSP00000262340.5:p.Val459=
ENST00000262340.5:c.1376T= ENSP00000262340.5:p.Val459=
NM_000329.2:c.1376T= NP_000320.1:p.Val459=
XM_017002027.1:c.1100T= XP_016857516.1:p.Val367=
NM_000329.3:c.1376T= MANE Select NP_000320.1:p.Val459=