Canonical Allele Identifier: CA1143700994
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68444576G= , CM000663.2:g.68444576G= GRCh38
NC_000001.10:g.68910259G= , CM000663.1:g.68910259G= GRCh37
NC_000001.9:g.68682847G= NCBI36
NG_008472.1:g.10384C=
NG_008472.2:g.10384C=

Transcript Alleles

HGVS Amino-acid change
ENST00000262340.6:c.450C= MANE Select ENSP00000262340.5:p.Asn150=
ENST00000262340.5:c.450C= ENSP00000262340.5:p.Asn150=
NM_000329.2:c.450C= NP_000320.1:p.Asn150=
XM_017002027.1:c.174C= XP_016857516.1:p.Asn58=
NM_000329.3:c.450C= MANE Select NP_000320.1:p.Asn150=