Canonical Allele Identifier: CA1401208079
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530466_129530467delinsCA , CM000665.2:g.129530466_129530467delinsCA GRCh38
NC_000003.11:g.129249309_129249310delinsCA , CM000665.1:g.129249309_129249310delinsCA GRCh37
NC_000003.10:g.130731999_130732000delinsCA NCBI36
NG_009115.1:g.6828_6829delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-410_362-409delinsCA MANE Select ENSP00000296271.3:n.362-410_362-409delinsCA
ENST00000296271.3:c.362-410_362-409delinsCA ENSP00000296271.3:n.362-410_362-409delinsCA
NM_000539.3:c.362-410_362-409delinsCA MANE Select NP_000530.1:n.362-410_362-409delinsCA