Canonical Allele Identifier: CA1173557434
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68429841C= , CM000663.2:g.68429841C= GRCh38
NC_000001.10:g.68895524C= , CM000663.1:g.68895524C= GRCh37
NC_000001.9:g.68668112C= NCBI36
NG_008472.1:g.25119G=
NG_008472.2:g.25119G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1537G= MANE Select ENSP00000262340.5:p.Val513=
ENST00000262340.5:c.1537G= ENSP00000262340.5:p.Val513=
NM_000329.2:c.1537G= NP_000320.1:p.Val513=
XM_017002027.1:c.1261G= XP_016857516.1:p.Val421=
NM_000329.3:c.1537G= MANE Select NP_000320.1:p.Val513=