Canonical Allele Identifier: CA2774965037

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096678_33096679del , CM000669.2:g.33096678_33096679del	GRCh38
NC_000007.13:g.33136290_33136291del , CM000669.1:g.33136290_33136291del	GRCh37
NC_000007.12:g.33102815_33102816del	NCBI36
NG_012968.1:g.17712_17713del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-125_2379-124del
ENST00000492391.2:n.1530-125_1530-124del
ENST00000682645.1:n.3477-125_3477-124del
ENST00000683432.1:c.*581-125_*581-124del	ENSP00000508174.1:n.*581-125_*581-124del
ENST00000684207.1:c.406-125_406-124del	ENSP00000506942.1:n.406-125_406-124del
ENST00000297157.8:c.406-125_406-124del MANE Select	ENSP00000297157.3:n.406-125_406-124del
ENST00000297157.7:c.406-125_406-124del	ENSP00000297157.3:n.406-125_406-124del
ENST00000448915.1:c.304-125_304-124del	ENSP00000411577.1:n.304-125_304-124del
NM_203288.1:c.406-125_406-124del	NP_976033.1:n.406-125_406-124del
XM_011515468.1:c.304-125_304-124del	XP_011513770.1:n.304-125_304-124del
XM_011515468.3:c.304-125_304-124del	XP_011513770.1:n.304-125_304-124del
NM_203288.2:c.406-125_406-124del MANE Select	NP_976033.1:n.406-125_406-124del