Canonical Allele Identifier: CA1173561339
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68439498G= , CM000663.2:g.68439498G= GRCh38
NC_000001.10:g.68905181G= , CM000663.1:g.68905181G= GRCh37
NC_000001.9:g.68677769G= NCBI36
NG_008472.1:g.15462C=
NG_008472.2:g.15462C=

Transcript Alleles

HGVS Amino-acid change
ENST00000262340.6:c.725+63C= MANE Select ENSP00000262340.5:n.725+63C=
ENST00000262340.5:c.725+63C= ENSP00000262340.5:n.725+63C=
NM_000329.2:c.725+63C= NP_000320.1:n.725+63C=
XM_017002027.1:c.449+63C= XP_016857516.1:n.449+63C=
NM_000329.3:c.725+63C= MANE Select NP_000320.1:n.725+63C=