Canonical Allele Identifier: CA340742394
Gene: RPE65 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431296A>C , CM000663.2:g.68431296A>C GRCh38
NC_000001.10:g.68896979A>C , CM000663.1:g.68896979A>C GRCh37
NC_000001.9:g.68669567A>C NCBI36
NG_008472.1:g.23664T>G
NG_008472.2:g.23664T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1324T>G MANE Select ENSP00000262340.5:p.Phe442Val
ENST00000262340.5:c.1324T>G ENSP00000262340.5:p.Phe442Val
NM_000329.2:c.1324T>G NP_000320.1:p.Phe442Val
XM_017002027.1:c.1048T>G XP_016857516.1:p.Phe350Val
NM_000329.3:c.1324T>G MANE Select NP_000320.1:p.Phe442Val