Canonical Allele Identifier: CA418277709
Gene: RPE65 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.68896992A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431309A>T , CM000663.2:g.68431309A>T GRCh38
NC_000001.10:g.68896992A>T , CM000663.1:g.68896992A>T GRCh37
NC_000001.9:g.68669580A>T NCBI36
NG_008472.1:g.23651T>A
NG_008472.2:g.23651T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1311T>A MANE Select ENSP00000262340.5:p.Leu437=
ENST00000262340.5:c.1311T>A ENSP00000262340.5:p.Leu437=
NM_000329.2:c.1311T>A NP_000320.1:p.Leu437=
XM_017002027.1:c.1035T>A XP_016857516.1:p.Leu345=
NM_000329.3:c.1311T>A MANE Select NP_000320.1:p.Leu437=