Canonical Allele Identifier: CA1173561146
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68438986A= , CM000663.2:g.68438986A= GRCh38
NC_000001.10:g.68904669A= , CM000663.1:g.68904669A= GRCh37
NC_000001.9:g.68677257A= NCBI36
NG_008472.1:g.15974T=
NG_008472.2:g.15974T=

Transcript Alleles

HGVS Amino-acid change
ENST00000262340.6:c.954T= MANE Select ENSP00000262340.5:p.Tyr318=
ENST00000262340.5:c.954T= ENSP00000262340.5:p.Tyr318=
NM_000329.2:c.954T= NP_000320.1:p.Tyr318=
XM_017002027.1:c.678T= XP_016857516.1:p.Tyr226=
NM_000329.3:c.954T= MANE Select NP_000320.1:p.Tyr318=