Canonical Allele Identifier: CA2758363677

Gene: RHO

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129529159_129529160insAGA , CM000665.2:g.129529159_129529160insAGA	GRCh38
NC_000003.11:g.129248002_129248003insAGA , CM000665.1:g.129248002_129248003insAGA	GRCh37
NC_000003.10:g.130730692_130730693insAGA	NCBI36
NG_009115.1:g.5521_5522insAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296271.4:c.361+65_361+66insAGA MANE Select	ENSP00000296271.3:n.361+65_361+66insAGA
ENST00000296271.3:c.361+65_361+66insAGA	ENSP00000296271.3:n.361+65_361+66insAGA
NM_000539.3:c.361+65_361+66insAGA MANE Select	NP_000530.1:n.361+65_361+66insAGA