Canonical Allele Identifier: CA2774965079

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096735_33096747del , CM000669.2:g.33096735_33096747del	GRCh38
NC_000007.13:g.33136347_33136359del , CM000669.1:g.33136347_33136359del	GRCh37
NC_000007.12:g.33102872_33102884del	NCBI36
NG_012968.1:g.17644_17656del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-193_2379-181del
ENST00000492391.2:n.1530-193_1530-181del
ENST00000682645.1:n.3477-193_3477-181del
ENST00000683432.1:c.*581-193_*581-181del	ENSP00000508174.1:n.*581-193_*581-181del
ENST00000684207.1:c.406-193_406-181del	ENSP00000506942.1:n.406-193_406-181del
ENST00000297157.8:c.406-193_406-181del MANE Select	ENSP00000297157.3:n.406-193_406-181del
ENST00000297157.7:c.406-193_406-181del	ENSP00000297157.3:n.406-193_406-181del
ENST00000448915.1:c.304-193_304-181del	ENSP00000411577.1:n.304-193_304-181del
NM_203288.1:c.406-193_406-181del	NP_976033.1:n.406-193_406-181del
XM_011515468.1:c.304-193_304-181del	XP_011513770.1:n.304-193_304-181del
XM_011515468.3:c.304-193_304-181del	XP_011513770.1:n.304-193_304-181del
NM_203288.2:c.406-193_406-181del MANE Select	NP_976033.1:n.406-193_406-181del