Canonical Allele Identifier: CA2744008997
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68429951_68429958del , CM000663.2:g.68429951_68429958del GRCh38
NC_000001.10:g.68895634_68895641del , CM000663.1:g.68895634_68895641del GRCh37
NC_000001.9:g.68668222_68668229del NCBI36
NG_008472.1:g.25003_25010del
NG_008472.2:g.25003_25010del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1451-30_1451-23del MANE Select ENSP00000262340.5:n.1451-30_1451-23del
ENST00000262340.5:c.1451-30_1451-23del ENSP00000262340.5:n.1451-30_1451-23del
NM_000329.2:c.1451-30_1451-23del NP_000320.1:n.1451-30_1451-23del
XM_017002027.1:c.1175-30_1175-23del XP_016857516.1:n.1175-30_1175-23del
NM_000329.3:c.1451-30_1451-23del MANE Select NP_000320.1:n.1451-30_1451-23del