Canonical Allele Identifier: CA2646149589
Gene: RPE65 HGNC NCBI

Linked Data

gnomAD v4: 1-68429660-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68429660C>A , CM000663.2:g.68429660C>A GRCh38
NC_000001.10:g.68895343C>A , CM000663.1:g.68895343C>A GRCh37
NC_000001.9:g.68667931C>A NCBI36
NG_008472.1:g.25300G>T
NG_008472.2:g.25300G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.*116G>T MANE Select ENSP00000262340.5:n.*116G>T
ENST00000262340.5:c.*116G>T ENSP00000262340.5:n.*116G>T
NM_000329.2:c.*116G>T NP_000320.1:n.*116G>T
XM_017002027.1:c.*116G>T XP_016857516.1:n.*116G>T
NM_000329.3:c.*116G>T MANE Select NP_000320.1:n.*116G>T