Canonical Allele Identifier: CA1173557361
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68429632T= , CM000663.2:g.68429632T= GRCh38
NC_000001.10:g.68895315T= , CM000663.1:g.68895315T= GRCh37
NC_000001.9:g.68667903T= NCBI36
NG_008472.1:g.25328A=
NG_008472.2:g.25328A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.*144A= MANE Select ENSP00000262340.5:n.*144A=
ENST00000262340.5:c.*144A= ENSP00000262340.5:n.*144A=
NM_000329.2:c.*144A= NP_000320.1:n.*144A=
XM_017002027.1:c.*144A= XP_016857516.1:n.*144A=
NM_000329.3:c.*144A= MANE Select NP_000320.1:n.*144A=