Canonical Allele Identifier: CA1173563396
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68444575A= , CM000663.2:g.68444575A= GRCh38
NC_000001.10:g.68910258A= , CM000663.1:g.68910258A= GRCh37
NC_000001.9:g.68682846A= NCBI36
NG_008472.1:g.10385T=
NG_008472.2:g.10385T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.451T= MANE Select ENSP00000262340.5:p.Phe151=
ENST00000262340.5:c.451T= ENSP00000262340.5:p.Phe151=
NM_000329.2:c.451T= NP_000320.1:p.Phe151=
XM_017002027.1:c.175T= XP_016857516.1:p.Phe59=
NM_000329.3:c.451T= MANE Select NP_000320.1:p.Phe151=