Canonical Allele Identifier: CA1173557942
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431168C= , CM000663.2:g.68431168C= GRCh38
NC_000001.10:g.68896851C= , CM000663.1:g.68896851C= GRCh37
NC_000001.9:g.68669439C= NCBI36
NG_008472.1:g.23792G=
NG_008472.2:g.23792G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1347G= MANE Select ENSP00000262340.5:p.Lys449=
ENST00000262340.5:c.1347G= ENSP00000262340.5:p.Lys449=
NM_000329.2:c.1347G= NP_000320.1:p.Lys449=
XM_017002027.1:c.1071G= XP_016857516.1:p.Lys357=
NM_000329.3:c.1347G= MANE Select NP_000320.1:p.Lys449=