Canonical Allele Identifier: CA1053435452
Gene: RHO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530533_129530534insCCACACACACACACACAC , CM000665.2:g.129530533_129530534insCCACACACACACACACAC GRCh38
NC_000003.11:g.129249376_129249377insCCACACACACACACACAC , CM000665.1:g.129249376_129249377insCCACACACACACACACAC GRCh37
NC_000003.10:g.130732066_130732067insCCACACACACACACACAC NCBI36
NG_009115.1:g.6895_6896insCCACACACACACACACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-343_362-342insCCACACACACACACACAC MANE Select ENSP00000296271.3:n.362-343_362-342insCCACACACACACACACAC
ENST00000296271.3:c.362-343_362-342insCCACACACACACACACAC ENSP00000296271.3:n.362-343_362-342insCCACACACACACACACAC
NM_000539.3:c.362-343_362-342insCCACACACACACACACAC MANE Select NP_000530.1:n.362-343_362-342insCCACACACACACACACAC