Canonical Allele Identifier: CA1173558057
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431485_68431486delinsGA , CM000663.2:g.68431485_68431486delinsGA GRCh38
NC_000001.10:g.68897168_68897169delinsGA , CM000663.1:g.68897168_68897169delinsGA GRCh37
NC_000001.9:g.68669756_68669757delinsGA NCBI36
NG_008472.1:g.23474_23475delinsTC
NG_008472.2:g.23474_23475delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1228_1229delinsTC MANE Select ENSP00000262340.5:p.Ser410=
ENST00000262340.5:c.1228_1229delinsTC ENSP00000262340.5:p.Ser410=
NM_000329.2:c.1228_1229delinsTC NP_000320.1:p.Ser410=
XM_017002027.1:c.952_953delinsTC XP_016857516.1:p.Ser318=
NM_000329.3:c.1228_1229delinsTC MANE Select NP_000320.1:p.Ser410=