Canonical Allele Identifier: CA2774964971

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096628_33096629insAG , CM000669.2:g.33096628_33096629insAG	GRCh38
NC_000007.13:g.33136240_33136241insAG , CM000669.1:g.33136240_33136241insAG	GRCh37
NC_000007.12:g.33102765_33102766insAG	NCBI36
NG_012968.1:g.17762_17763insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-75_2379-74insCT
ENST00000492391.2:n.1530-75_1530-74insCT
ENST00000682645.1:n.3477-75_3477-74insCT
ENST00000683432.1:c.*581-75_*581-74insCT	ENSP00000508174.1:n.*581-75_*581-74insCT
ENST00000684207.1:c.406-75_406-74insCT	ENSP00000506942.1:n.406-75_406-74insCT
ENST00000297157.8:c.406-75_406-74insCT MANE Select	ENSP00000297157.3:n.406-75_406-74insCT
ENST00000297157.7:c.406-75_406-74insCT	ENSP00000297157.3:n.406-75_406-74insCT
ENST00000448915.1:c.304-75_304-74insCT	ENSP00000411577.1:n.304-75_304-74insCT
NM_203288.1:c.406-75_406-74insCT	NP_976033.1:n.406-75_406-74insCT
XM_011515468.1:c.304-75_304-74insCT	XP_011513770.1:n.304-75_304-74insCT
XM_011515468.3:c.304-75_304-74insCT	XP_011513770.1:n.304-75_304-74insCT
NM_203288.2:c.406-75_406-74insCT MANE Select	NP_976033.1:n.406-75_406-74insCT