Canonical Allele Identifier: CA1173564230
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68446748C= , CM000663.2:g.68446748C= GRCh38
NC_000001.10:g.68912431C= , CM000663.1:g.68912431C= GRCh37
NC_000001.9:g.68685019C= NCBI36
NG_008472.1:g.8212G=
NG_008472.2:g.8212G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.207G= MANE Select ENSP00000262340.5:p.Lys69=
ENST00000262340.5:c.207G= ENSP00000262340.5:p.Lys69=
NM_000329.2:c.207G= NP_000320.1:p.Lys69=
XM_017002027.1:c.-31-1865G= XP_016857516.1:n.-31-1865G=
NM_000329.3:c.207G= MANE Select NP_000320.1:p.Lys69=