Canonical Allele Identifier: CA2744009056
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68430046_68430047insA , CM000663.2:g.68430046_68430047insA GRCh38
NC_000001.10:g.68895729_68895730insA , CM000663.1:g.68895729_68895730insA GRCh37
NC_000001.9:g.68668317_68668318insA NCBI36
NG_008472.1:g.24913_24914insT
NG_008472.2:g.24913_24914insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1451-120_1451-119insT MANE Select ENSP00000262340.5:n.1451-120_1451-119insT
ENST00000262340.5:c.1451-120_1451-119insT ENSP00000262340.5:n.1451-120_1451-119insT
NM_000329.2:c.1451-120_1451-119insT NP_000320.1:n.1451-120_1451-119insT
XM_017002027.1:c.1175-120_1175-119insT XP_016857516.1:n.1175-120_1175-119insT
NM_000329.3:c.1451-120_1451-119insT MANE Select NP_000320.1:n.1451-120_1451-119insT