Canonical Allele Identifier: CA1401208065
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530448_129530449delinsCT , CM000665.2:g.129530448_129530449delinsCT GRCh38
NC_000003.11:g.129249291_129249292delinsCT , CM000665.1:g.129249291_129249292delinsCT GRCh37
NC_000003.10:g.130731981_130731982delinsCT NCBI36
NG_009115.1:g.6810_6811delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-428_362-427delinsCT MANE Select ENSP00000296271.3:n.362-428_362-427delinsCT
ENST00000296271.3:c.362-428_362-427delinsCT ENSP00000296271.3:n.362-428_362-427delinsCT
NM_000539.3:c.362-428_362-427delinsCT MANE Select NP_000530.1:n.362-428_362-427delinsCT