Canonical Allele Identifier: CA2518422143
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431239_68431240insG , CM000663.2:g.68431239_68431240insG GRCh38
NC_000001.10:g.68896922_68896923insG , CM000663.1:g.68896922_68896923insG GRCh37
NC_000001.9:g.68669510_68669511insG NCBI36
NG_008472.1:g.23720_23721insC
NG_008472.2:g.23720_23721insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1338+42_1338+43insC MANE Select ENSP00000262340.5:n.1338+42_1338+43insC
ENST00000262340.5:c.1338+42_1338+43insC ENSP00000262340.5:n.1338+42_1338+43insC
NM_000329.2:c.1338+42_1338+43insC NP_000320.1:n.1338+42_1338+43insC
XM_017002027.1:c.1062+42_1062+43insC XP_016857516.1:n.1062+42_1062+43insC
NM_000329.3:c.1338+42_1338+43insC MANE Select NP_000320.1:n.1338+42_1338+43insC