Canonical Allele Identifier: CA1401208819
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530536_129530539delinsACAC , CM000665.2:g.129530536_129530539delinsACAC GRCh38
NC_000003.11:g.129249379_129249382delinsACAC , CM000665.1:g.129249379_129249382delinsACAC GRCh37
NC_000003.10:g.130732069_130732072delinsACAC NCBI36
NG_009115.1:g.6898_6901delinsACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-340_362-337delinsACAC MANE Select ENSP00000296271.3:n.362-340_362-337delinsACAC
ENST00000296271.3:c.362-340_362-337delinsACAC ENSP00000296271.3:n.362-340_362-337delinsACAC
NM_000539.3:c.362-340_362-337delinsACAC MANE Select NP_000530.1:n.362-340_362-337delinsACAC