Canonical Allele Identifier: CA340748103
Gene: RPE65 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68444782A>T , CM000663.2:g.68444782A>T GRCh38
NC_000001.10:g.68910465A>T , CM000663.1:g.68910465A>T GRCh37
NC_000001.9:g.68683053A>T NCBI36
NG_008472.1:g.10178T>A
NG_008472.2:g.10178T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.347T>A MANE Select ENSP00000262340.5:p.Phe116Tyr
ENST00000262340.5:c.347T>A ENSP00000262340.5:p.Phe116Tyr
NM_000329.2:c.347T>A NP_000320.1:p.Phe116Tyr
XM_017002027.1:c.71T>A XP_016857516.1:p.Phe24Tyr
NM_000329.3:c.347T>A MANE Select NP_000320.1:p.Phe116Tyr