Canonical Allele Identifier: CA1401208893
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530567_129530569delinsCAA , CM000665.2:g.129530567_129530569delinsCAA GRCh38
NC_000003.11:g.129249410_129249412delinsCAA , CM000665.1:g.129249410_129249412delinsCAA GRCh37
NC_000003.10:g.130732100_130732102delinsCAA NCBI36
NG_009115.1:g.6929_6931delinsCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-309_362-307delinsCAA MANE Select ENSP00000296271.3:n.362-309_362-307delinsCAA
ENST00000296271.3:c.362-309_362-307delinsCAA ENSP00000296271.3:n.362-309_362-307delinsCAA
NM_000539.3:c.362-309_362-307delinsCAA MANE Select NP_000530.1:n.362-309_362-307delinsCAA