Canonical Allele Identifier: CA1143362880
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431479G= , CM000663.2:g.68431479G= GRCh38
NC_000001.10:g.68897162G= , CM000663.1:g.68897162G= GRCh37
NC_000001.9:g.68669750G= NCBI36
NG_008472.1:g.23481C=
NG_008472.2:g.23481C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1235C= MANE Select ENSP00000262340.5:p.Pro412=
ENST00000262340.5:c.1235C= ENSP00000262340.5:p.Pro412=
NM_000329.2:c.1235C= NP_000320.1:p.Pro412=
XM_017002027.1:c.959C= XP_016857516.1:p.Pro320=
NM_000329.3:c.1235C= MANE Select NP_000320.1:p.Pro412=