Canonical Allele Identifier: CA1143450873
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431476C= , CM000663.2:g.68431476C= GRCh38
NC_000001.10:g.68897159C= , CM000663.1:g.68897159C= GRCh37
NC_000001.9:g.68669747C= NCBI36
NG_008472.1:g.23484G=
NG_008472.2:g.23484G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1238G= MANE Select ENSP00000262340.5:p.Arg413=
ENST00000262340.5:c.1238G= ENSP00000262340.5:p.Arg413=
NM_000329.2:c.1238G= NP_000320.1:p.Arg413=
XM_017002027.1:c.962G= XP_016857516.1:p.Arg321=
NM_000329.3:c.1238G= MANE Select NP_000320.1:p.Arg413=