Canonical Allele Identifier: CA2560722070
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530568_129530569insCATA , CM000665.2:g.129530568_129530569insCATA GRCh38
NC_000003.11:g.129249411_129249412insCATA , CM000665.1:g.129249411_129249412insCATA GRCh37
NC_000003.10:g.130732101_130732102insCATA NCBI36
NG_009115.1:g.6930_6931insCATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-308_362-307insCATA MANE Select ENSP00000296271.3:n.362-308_362-307insCATA
ENST00000296271.3:c.362-308_362-307insCATA ENSP00000296271.3:n.362-308_362-307insCATA
NM_000539.3:c.362-308_362-307insCATA MANE Select NP_000530.1:n.362-308_362-307insCATA