Canonical Allele Identifier: CA1401208263
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530531_129530545delinsACAACACACACACAC , CM000665.2:g.129530531_129530545delinsACAACACACACACAC GRCh38
NC_000003.11:g.129249374_129249388delinsACAACACACACACAC , CM000665.1:g.129249374_129249388delinsACAACACACACACAC GRCh37
NC_000003.10:g.130732064_130732078delinsACAACACACACACAC NCBI36
NG_009115.1:g.6893_6907delinsACAACACACACACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-345_362-331delinsACAACACACACACAC MANE Select ENSP00000296271.3:n.362-345_362-331delinsACAACACACACACAC
ENST00000296271.3:c.362-345_362-331delinsACAACACACACACAC ENSP00000296271.3:n.362-345_362-331delinsACAACACACACACAC
NM_000539.3:c.362-345_362-331delinsACAACACACACACAC MANE Select NP_000530.1:n.362-345_362-331delinsACAACACACACACAC