Canonical Allele Identifier: CA1173561148
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68438989G= , CM000663.2:g.68438989G= GRCh38
NC_000001.10:g.68904672G= , CM000663.1:g.68904672G= GRCh37
NC_000001.9:g.68677260G= NCBI36
NG_008472.1:g.15971C=
NG_008472.2:g.15971C=

Transcript Alleles

HGVS Amino-acid change
ENST00000262340.6:c.951C= MANE Select ENSP00000262340.5:p.Thr317=
ENST00000262340.5:c.951C= ENSP00000262340.5:p.Thr317=
NM_000329.2:c.951C= NP_000320.1:p.Thr317=
XM_017002027.1:c.675C= XP_016857516.1:p.Thr225=
NM_000329.3:c.951C= MANE Select NP_000320.1:p.Thr317=