Canonical Allele Identifier: CA1173563381
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68444540T= , CM000663.2:g.68444540T= GRCh38
NC_000001.10:g.68910223T= , CM000663.1:g.68910223T= GRCh37
NC_000001.9:g.68682811T= NCBI36
NG_008472.1:g.10420A=
NG_008472.2:g.10420A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.486A= MANE Select ENSP00000262340.5:p.Thr162=
ENST00000262340.5:c.486A= ENSP00000262340.5:p.Thr162=
NM_000329.2:c.486A= NP_000320.1:p.Thr162=
XM_017002027.1:c.210A= XP_016857516.1:p.Thr70=
NM_000329.3:c.486A= MANE Select NP_000320.1:p.Thr162=