Canonical Allele Identifier: CA1173560849
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68438219T= , CM000663.2:g.68438219T= GRCh38
NC_000001.10:g.68903902T= , CM000663.1:g.68903902T= GRCh37
NC_000001.9:g.68676490T= NCBI36
NG_008472.1:g.16741A=
NG_008472.2:g.16741A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1096A= MANE Select ENSP00000262340.5:p.Arg366=
ENST00000262340.5:c.1096A= ENSP00000262340.5:p.Arg366=
NM_000329.2:c.1096A= NP_000320.1:p.Arg366=
XM_017002027.1:c.820A= XP_016857516.1:p.Arg274=
NM_000329.3:c.1096A= MANE Select NP_000320.1:p.Arg366=