Canonical Allele Identifier: CA2744009103
Gene: RPE65 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431445G>T , CM000663.2:g.68431445G>T GRCh38
NC_000001.10:g.68897128G>T , CM000663.1:g.68897128G>T GRCh37
NC_000001.9:g.68669716G>T NCBI36
NG_008472.1:g.23515C>A
NG_008472.2:g.23515C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1243+26C>A MANE Select ENSP00000262340.5:n.1243+26C>A
ENST00000262340.5:c.1243+26C>A ENSP00000262340.5:n.1243+26C>A
NM_000329.2:c.1243+26C>A NP_000320.1:n.1243+26C>A
XM_017002027.1:c.967+26C>A XP_016857516.1:n.967+26C>A
NM_000329.3:c.1243+26C>A MANE Select NP_000320.1:n.1243+26C>A
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