Canonical Allele Identifier: CA1173563432
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68444671A= , CM000663.2:g.68444671A= GRCh38
NC_000001.10:g.68910354A= , CM000663.1:g.68910354A= GRCh37
NC_000001.9:g.68682942A= NCBI36
NG_008472.1:g.10289T=
NG_008472.2:g.10289T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.355T= MANE Select ENSP00000262340.5:p.Phe119=
ENST00000262340.5:c.355T= ENSP00000262340.5:p.Phe119=
NM_000329.2:c.355T= NP_000320.1:p.Phe119=
XM_017002027.1:c.79T= XP_016857516.1:p.Phe27=
NM_000329.3:c.355T= MANE Select NP_000320.1:p.Phe119=