Canonical Allele Identifier: CA1142494686
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431212G= , CM000663.2:g.68431212G= GRCh38
NC_000001.10:g.68896895G= , CM000663.1:g.68896895G= GRCh37
NC_000001.9:g.68669483G= NCBI36
NG_008472.1:g.23748C=
NG_008472.2:g.23748C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1339-36C= MANE Select ENSP00000262340.5:n.1339-36C=
ENST00000262340.5:c.1339-36C= ENSP00000262340.5:n.1339-36C=
NM_000329.2:c.1339-36C= NP_000320.1:n.1339-36C=
XM_017002027.1:c.1063-36C= XP_016857516.1:n.1063-36C=
NM_000329.3:c.1339-36C= MANE Select NP_000320.1:n.1339-36C=