Canonical Allele Identifier: CA1173557941
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431164T= , CM000663.2:g.68431164T= GRCh38
NC_000001.10:g.68896847T= , CM000663.1:g.68896847T= GRCh37
NC_000001.9:g.68669435T= NCBI36
NG_008472.1:g.23796A=
NG_008472.2:g.23796A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1351A= MANE Select ENSP00000262340.5:p.Asn451=
ENST00000262340.5:c.1351A= ENSP00000262340.5:p.Asn451=
NM_000329.2:c.1351A= NP_000320.1:p.Asn451=
XM_017002027.1:c.1075A= XP_016857516.1:p.Asn359=
NM_000329.3:c.1351A= MANE Select NP_000320.1:p.Asn451=