Canonical Allele Identifier: CA1173557930
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431127G= , CM000663.2:g.68431127G= GRCh38
NC_000001.10:g.68896810G= , CM000663.1:g.68896810G= GRCh37
NC_000001.9:g.68669398G= NCBI36
NG_008472.1:g.23833C=
NG_008472.2:g.23833C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1388C= MANE Select ENSP00000262340.5:p.Pro463=
ENST00000262340.5:c.1388C= ENSP00000262340.5:p.Pro463=
NM_000329.2:c.1388C= NP_000320.1:p.Pro463=
XM_017002027.1:c.1112C= XP_016857516.1:p.Pro371=
NM_000329.3:c.1388C= MANE Select NP_000320.1:p.Pro463=