Canonical Allele Identifier: CA1140762638
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431316T= , CM000663.2:g.68431316T= GRCh38
NC_000001.10:g.68896999T= , CM000663.1:g.68896999T= GRCh37
NC_000001.9:g.68669587T= NCBI36
NG_008472.1:g.23644A=
NG_008472.2:g.23644A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1304A= MANE Select ENSP00000262340.5:p.Tyr435=
ENST00000262340.5:c.1304A= ENSP00000262340.5:p.Tyr435=
NM_000329.2:c.1304A= NP_000320.1:p.Tyr435=
XM_017002027.1:c.1028A= XP_016857516.1:p.Tyr343=
NM_000329.3:c.1304A= MANE Select NP_000320.1:p.Tyr435=