Canonical Allele Identifier: CA1401208120
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530506_129530518delinsAACACACACACAC , CM000665.2:g.129530506_129530518delinsAACACACACACAC GRCh38
NC_000003.11:g.129249349_129249361delinsAACACACACACAC , CM000665.1:g.129249349_129249361delinsAACACACACACAC GRCh37
NC_000003.10:g.130732039_130732051delinsAACACACACACAC NCBI36
NG_009115.1:g.6868_6880delinsAACACACACACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-370_362-358delinsAACACACACACAC MANE Select ENSP00000296271.3:n.362-370_362-358delinsAACACACACACAC
ENST00000296271.3:c.362-370_362-358delinsAACACACACACAC ENSP00000296271.3:n.362-370_362-358delinsAACACACACACAC
NM_000539.3:c.362-370_362-358delinsAACACACACACAC MANE Select NP_000530.1:n.362-370_362-358delinsAACACACACACAC