Canonical Allele Identifier: CA1401208183
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530523_129530528delinsACACAC , CM000665.2:g.129530523_129530528delinsACACAC GRCh38
NC_000003.11:g.129249366_129249371delinsACACAC , CM000665.1:g.129249366_129249371delinsACACAC GRCh37
NC_000003.10:g.130732056_130732061delinsACACAC NCBI36
NG_009115.1:g.6885_6890delinsACACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-353_362-348delinsACACAC MANE Select ENSP00000296271.3:n.362-353_362-348delinsACACAC
ENST00000296271.3:c.362-353_362-348delinsACACAC ENSP00000296271.3:n.362-353_362-348delinsACACAC
NM_000539.3:c.362-353_362-348delinsACACAC MANE Select NP_000530.1:n.362-353_362-348delinsACACAC