Canonical Allele Identifier: CA1173557369
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68429648C= , CM000663.2:g.68429648C= GRCh38
NC_000001.10:g.68895331C= , CM000663.1:g.68895331C= GRCh37
NC_000001.9:g.68667919C= NCBI36
NG_008472.1:g.25312G=
NG_008472.2:g.25312G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.*128G= MANE Select ENSP00000262340.5:n.*128G=
ENST00000262340.5:c.*128G= ENSP00000262340.5:n.*128G=
NM_000329.2:c.*128G= NP_000320.1:n.*128G=
XM_017002027.1:c.*128G= XP_016857516.1:n.*128G=
NM_000329.3:c.*128G= MANE Select NP_000320.1:n.*128G=