Canonical Allele Identifier: CA2646150117
Gene: RPE65 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431248del , CM000663.2:g.68431248del GRCh38
NC_000001.10:g.68896931del , CM000663.1:g.68896931del GRCh37
NC_000001.9:g.68669519del NCBI36
NG_008472.1:g.23712del
NG_008472.2:g.23712del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1338+34del MANE Select ENSP00000262340.5:n.1338+34del
ENST00000262340.5:c.1338+34del ENSP00000262340.5:n.1338+34del
NM_000329.2:c.1338+34del NP_000320.1:n.1338+34del
XM_017002027.1:c.1062+34del XP_016857516.1:n.1062+34del
NM_000329.3:c.1338+34del MANE Select NP_000320.1:n.1338+34del