Canonical Allele Identifier: CA2774965010

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096662_33096663insA , CM000669.2:g.33096662_33096663insA	GRCh38
NC_000007.13:g.33136274_33136275insA , CM000669.1:g.33136274_33136275insA	GRCh37
NC_000007.12:g.33102799_33102800insA	NCBI36
NG_012968.1:g.17728_17729insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-109_2379-108insT
ENST00000492391.2:n.1530-109_1530-108insT
ENST00000682645.1:n.3477-109_3477-108insT
ENST00000683432.1:c.*581-109_*581-108insT	ENSP00000508174.1:n.*581-109_*581-108insT
ENST00000684207.1:c.406-109_406-108insT	ENSP00000506942.1:n.406-109_406-108insT
ENST00000297157.8:c.406-109_406-108insT MANE Select	ENSP00000297157.3:n.406-109_406-108insT
ENST00000297157.7:c.406-109_406-108insT	ENSP00000297157.3:n.406-109_406-108insT
ENST00000448915.1:c.304-109_304-108insT	ENSP00000411577.1:n.304-109_304-108insT
NM_203288.1:c.406-109_406-108insT	NP_976033.1:n.406-109_406-108insT
XM_011515468.1:c.304-109_304-108insT	XP_011513770.1:n.304-109_304-108insT
XM_011515468.3:c.304-109_304-108insT	XP_011513770.1:n.304-109_304-108insT
NM_203288.2:c.406-109_406-108insT MANE Select	NP_976033.1:n.406-109_406-108insT