Canonical Allele Identifier: CA1173557950
Gene: RPE65 HGNC NCBI

Linked Data

dbSNP Id: rs1645823428

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.68431196dup , CM000663.2:g.68431196dup GRCh38
NC_000001.10:g.68896879dup , CM000663.1:g.68896879dup GRCh37
NC_000001.9:g.68669467dup NCBI36
NG_008472.1:g.23768dup
NG_008472.2:g.23768dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000262340.6:c.1339-16dup MANE Select ENSP00000262340.5:n.1339-16dup
ENST00000262340.5:c.1339-16dup ENSP00000262340.5:n.1339-16dup
NM_000329.2:c.1339-16dup NP_000320.1:n.1339-16dup
XM_017002027.1:c.1063-16dup XP_016857516.1:n.1063-16dup
NM_000329.3:c.1339-16dup MANE Select NP_000320.1:n.1339-16dup