Canonical Allele Identifier: CA1401210523
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129531899_129531900delinsCA , CM000665.2:g.129531899_129531900delinsCA GRCh38
NC_000003.11:g.129250742_129250743delinsCA , CM000665.1:g.129250742_129250743delinsCA GRCh37
NC_000003.10:g.130733432_130733433delinsCA NCBI36
NG_009115.1:g.8261_8262delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.531-352_531-351delinsCA MANE Select ENSP00000296271.3:n.531-352_531-351delinsCA
ENST00000296271.3:c.531-352_531-351delinsCA ENSP00000296271.3:n.531-352_531-351delinsCA
NM_000539.3:c.531-352_531-351delinsCA MANE Select NP_000530.1:n.531-352_531-351delinsCA