Canonical Allele Identifier: CA1173558033
Gene: RPE65 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431430T= , CM000663.2:g.68431430T= GRCh38
NC_000001.10:g.68897113T= , CM000663.1:g.68897113T= GRCh37
NC_000001.9:g.68669701T= NCBI36
NG_008472.1:g.23530A=
NG_008472.2:g.23530A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1243+41A= MANE Select ENSP00000262340.5:n.1243+41A=
ENST00000262340.5:c.1243+41A= ENSP00000262340.5:n.1243+41A=
NM_000329.2:c.1243+41A= NP_000320.1:n.1243+41A=
XM_017002027.1:c.967+41A= XP_016857516.1:n.967+41A=
NM_000329.3:c.1243+41A= MANE Select NP_000320.1:n.1243+41A=