Canonical Allele Identifier: CA2744009059
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68430076_68430077insA , CM000663.2:g.68430076_68430077insA GRCh38
NC_000001.10:g.68895759_68895760insA , CM000663.1:g.68895759_68895760insA GRCh37
NC_000001.9:g.68668347_68668348insA NCBI36
NG_008472.1:g.24883_24884insT
NG_008472.2:g.24883_24884insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1451-150_1451-149insT MANE Select ENSP00000262340.5:n.1451-150_1451-149insT
ENST00000262340.5:c.1451-150_1451-149insT ENSP00000262340.5:n.1451-150_1451-149insT
NM_000329.2:c.1451-150_1451-149insT NP_000320.1:n.1451-150_1451-149insT
XM_017002027.1:c.1175-150_1175-149insT XP_016857516.1:n.1175-150_1175-149insT
NM_000329.3:c.1451-150_1451-149insT MANE Select NP_000320.1:n.1451-150_1451-149insT