Canonical Allele Identifier: CA1401208218
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530527_129530535delinsACACACAAC , CM000665.2:g.129530527_129530535delinsACACACAAC GRCh38
NC_000003.11:g.129249370_129249378delinsACACACAAC , CM000665.1:g.129249370_129249378delinsACACACAAC GRCh37
NC_000003.10:g.130732060_130732068delinsACACACAAC NCBI36
NG_009115.1:g.6889_6897delinsACACACAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-349_362-341delinsACACACAAC MANE Select ENSP00000296271.3:n.362-349_362-341delinsACACACAAC
ENST00000296271.3:c.362-349_362-341delinsACACACAAC ENSP00000296271.3:n.362-349_362-341delinsACACACAAC
NM_000539.3:c.362-349_362-341delinsACACACAAC MANE Select NP_000530.1:n.362-349_362-341delinsACACACAAC