Canonical Allele Identifier: CA1173564227
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68446742G= , CM000663.2:g.68446742G= GRCh38
NC_000001.10:g.68912425G= , CM000663.1:g.68912425G= GRCh37
NC_000001.9:g.68685013G= NCBI36
NG_008472.1:g.8218C=
NG_008472.2:g.8218C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.213C= MANE Select ENSP00000262340.5:p.Asp71=
ENST00000262340.5:c.213C= ENSP00000262340.5:p.Asp71=
NM_000329.2:c.213C= NP_000320.1:p.Asp71=
XM_017002027.1:c.-31-1859C= XP_016857516.1:n.-31-1859C=
NM_000329.3:c.213C= MANE Select NP_000320.1:p.Asp71=