Canonical Allele Identifier: CA1173557411
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68429757A= , CM000663.2:g.68429757A= GRCh38
NC_000001.10:g.68895440A= , CM000663.1:g.68895440A= GRCh37
NC_000001.9:g.68668028A= NCBI36
NG_008472.1:g.25203T=
NG_008472.2:g.25203T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.*19T= MANE Select ENSP00000262340.5:n.*19T=
ENST00000262340.5:c.*19T= ENSP00000262340.5:n.*19T=
NM_000329.2:c.*19T= NP_000320.1:n.*19T=
XM_017002027.1:c.*19T= XP_016857516.1:n.*19T=
NM_000329.3:c.*19T= MANE Select NP_000320.1:n.*19T=