Canonical Allele Identifier: CA902190
Gene: RPE65 HGNC NCBI

Linked Data

ClinVar Variation Id: 2926705
ClinVar RCV Id: RCV003788943
dbSNP Id: rs143435745
gnomAD v2: 1-68896841-T-C
gnomAD v3: 1-68431158-T-C
gnomAD v4: 1-68431158-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431158T>C , CM000663.2:g.68431158T>C GRCh38
NC_000001.10:g.68896841T>C , CM000663.1:g.68896841T>C GRCh37
NC_000001.9:g.68669429T>C NCBI36
NG_008472.1:g.23802A>G
NG_008472.2:g.23802A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1357A>G MANE Select ENSP00000262340.5:p.Lys453Glu
ENST00000262340.5:c.1357A>G ENSP00000262340.5:p.Lys453Glu
NM_000329.2:c.1357A>G NP_000320.1:p.Lys453Glu
XM_017002027.1:c.1081A>G XP_016857516.1:p.Lys361Glu
NM_000329.3:c.1357A>G MANE Select NP_000320.1:p.Lys453Glu