Canonical Allele Identifier: CA1173557525
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68430064_68430065delinsCT , CM000663.2:g.68430064_68430065delinsCT GRCh38
NC_000001.10:g.68895747_68895748delinsCT , CM000663.1:g.68895747_68895748delinsCT GRCh37
NC_000001.9:g.68668335_68668336delinsCT NCBI36
NG_008472.1:g.24895_24896delinsAG
NG_008472.2:g.24895_24896delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1451-138_1451-137delinsAG MANE Select ENSP00000262340.5:n.1451-138_1451-137delinsAG
ENST00000262340.5:c.1451-138_1451-137delinsAG ENSP00000262340.5:n.1451-138_1451-137delinsAG
NM_000329.2:c.1451-138_1451-137delinsAG NP_000320.1:n.1451-138_1451-137delinsAG
XM_017002027.1:c.1175-138_1175-137delinsAG XP_016857516.1:n.1175-138_1175-137delinsAG
NM_000329.3:c.1451-138_1451-137delinsAG MANE Select NP_000320.1:n.1451-138_1451-137delinsAG