Canonical Allele Identifier: CA2758363664

Gene: RHO

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129529101_129529102insACA , CM000665.2:g.129529101_129529102insACA	GRCh38
NC_000003.11:g.129247944_129247945insACA , CM000665.1:g.129247944_129247945insACA	GRCh37
NC_000003.10:g.130730634_130730635insACA	NCBI36
NG_009115.1:g.5463_5464insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296271.4:c.361+7_361+8insACA MANE Select	ENSP00000296271.3:n.361+7_361+8insACA
ENST00000296271.3:c.361+7_361+8insACA	ENSP00000296271.3:n.361+7_361+8insACA
NM_000539.3:c.361+7_361+8insACA MANE Select	NP_000530.1:n.361+7_361+8insACA