Canonical Allele Identifier: CA1173560873
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68438303A= , CM000663.2:g.68438303A= GRCh38
NC_000001.10:g.68903986A= , CM000663.1:g.68903986A= GRCh37
NC_000001.9:g.68676574A= NCBI36
NG_008472.1:g.16657T=
NG_008472.2:g.16657T=

Transcript Alleles

HGVS Amino-acid change
ENST00000262340.6:c.1012T= MANE Select ENSP00000262340.5:p.Tyr338=
ENST00000262340.5:c.1012T= ENSP00000262340.5:p.Tyr338=
NM_000329.2:c.1012T= NP_000320.1:p.Tyr338=
XM_017002027.1:c.736T= XP_016857516.1:p.Tyr246=
NM_000329.3:c.1012T= MANE Select NP_000320.1:p.Tyr338=