Canonical Allele Identifier: CA1146485358
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68429721C= , CM000663.2:g.68429721C= GRCh38
NC_000001.10:g.68895404C= , CM000663.1:g.68895404C= GRCh37
NC_000001.9:g.68667992C= NCBI36
NG_008472.1:g.25239G=
NG_008472.2:g.25239G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.*55G= MANE Select ENSP00000262340.5:n.*55G=
ENST00000262340.5:c.*55G= ENSP00000262340.5:n.*55G=
NM_000329.2:c.*55G= NP_000320.1:n.*55G=
XM_017002027.1:c.*55G= XP_016857516.1:n.*55G=
NM_000329.3:c.*55G= MANE Select NP_000320.1:n.*55G=