Canonical Allele Identifier: CA916200247
Gene: RPE65 HGNC NCBI

Linked Data

dbSNP Id: rs1571158509

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431272del , CM000663.2:g.68431272del GRCh38
NC_000001.10:g.68896955del , CM000663.1:g.68896955del GRCh37
NC_000001.9:g.68669543del NCBI36
NG_008472.1:g.23689del
NG_008472.2:g.23689del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1338+11del MANE Select ENSP00000262340.5:n.1338+11del
ENST00000262340.5:c.1338+11del ENSP00000262340.5:n.1338+11del
NM_000329.2:c.1338+11del NP_000320.1:n.1338+11del
XM_017002027.1:c.1062+11del XP_016857516.1:n.1062+11del
NM_000329.3:c.1338+11del MANE Select NP_000320.1:n.1338+11del