Canonical Allele Identifier: CA1401208097
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530482_129530492delinsACATTAGGATG , CM000665.2:g.129530482_129530492delinsACATTAGGATG GRCh38
NC_000003.11:g.129249325_129249335delinsACATTAGGATG , CM000665.1:g.129249325_129249335delinsACATTAGGATG GRCh37
NC_000003.10:g.130732015_130732025delinsACATTAGGATG NCBI36
NG_009115.1:g.6844_6854delinsACATTAGGATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-394_362-384delinsACATTAGGATG MANE Select ENSP00000296271.3:n.362-394_362-384delinsACATTAGGATG
ENST00000296271.3:c.362-394_362-384delinsACATTAGGATG ENSP00000296271.3:n.362-394_362-384delinsACATTAGGATG
NM_000539.3:c.362-394_362-384delinsACATTAGGATG MANE Select NP_000530.1:n.362-394_362-384delinsACATTAGGATG