Canonical Allele Identifier: CA1173557380
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68429677C= , CM000663.2:g.68429677C= GRCh38
NC_000001.10:g.68895360C= , CM000663.1:g.68895360C= GRCh37
NC_000001.9:g.68667948C= NCBI36
NG_008472.1:g.25283G=
NG_008472.2:g.25283G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.*99G= MANE Select ENSP00000262340.5:n.*99G=
ENST00000262340.5:c.*99G= ENSP00000262340.5:n.*99G=
NM_000329.2:c.*99G= NP_000320.1:n.*99G=
XM_017002027.1:c.*99G= XP_016857516.1:n.*99G=
NM_000329.3:c.*99G= MANE Select NP_000320.1:n.*99G=