Canonical Allele Identifier: CA1173558031
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431425A= , CM000663.2:g.68431425A= GRCh38
NC_000001.10:g.68897108A= , CM000663.1:g.68897108A= GRCh37
NC_000001.9:g.68669696A= NCBI36
NG_008472.1:g.23535T=
NG_008472.2:g.23535T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1243+46T= MANE Select ENSP00000262340.5:n.1243+46T=
ENST00000262340.5:c.1243+46T= ENSP00000262340.5:n.1243+46T=
NM_000329.2:c.1243+46T= NP_000320.1:n.1243+46T=
XM_017002027.1:c.967+46T= XP_016857516.1:n.967+46T=
NM_000329.3:c.1243+46T= MANE Select NP_000320.1:n.1243+46T=