Canonical Allele Identifier: CA2744009058
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68430076_68430081del , CM000663.2:g.68430076_68430081del GRCh38
NC_000001.10:g.68895759_68895764del , CM000663.1:g.68895759_68895764del GRCh37
NC_000001.9:g.68668347_68668352del NCBI36
NG_008472.1:g.24879_24884del
NG_008472.2:g.24879_24884del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1451-154_1451-149del MANE Select ENSP00000262340.5:n.1451-154_1451-149del
ENST00000262340.5:c.1451-154_1451-149del ENSP00000262340.5:n.1451-154_1451-149del
NM_000329.2:c.1451-154_1451-149del NP_000320.1:n.1451-154_1451-149del
XM_017002027.1:c.1175-154_1175-149del XP_016857516.1:n.1175-154_1175-149del
NM_000329.3:c.1451-154_1451-149del MANE Select NP_000320.1:n.1451-154_1451-149del