Canonical Allele Identifier: CA2774965031

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096675_33096678del , CM000669.2:g.33096675_33096678del	GRCh38
NC_000007.13:g.33136287_33136290del , CM000669.1:g.33136287_33136290del	GRCh37
NC_000007.12:g.33102812_33102815del	NCBI36
NG_012968.1:g.17713_17716del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-124_2379-121del
ENST00000492391.2:n.1530-124_1530-121del
ENST00000682645.1:n.3477-124_3477-121del
ENST00000683432.1:c.*581-124_*581-121del	ENSP00000508174.1:n.*581-124_*581-121del
ENST00000684207.1:c.406-124_406-121del	ENSP00000506942.1:n.406-124_406-121del
ENST00000297157.8:c.406-124_406-121del MANE Select	ENSP00000297157.3:n.406-124_406-121del
ENST00000297157.7:c.406-124_406-121del	ENSP00000297157.3:n.406-124_406-121del
ENST00000448915.1:c.304-124_304-121del	ENSP00000411577.1:n.304-124_304-121del
NM_203288.1:c.406-124_406-121del	NP_976033.1:n.406-124_406-121del
XM_011515468.1:c.304-124_304-121del	XP_011513770.1:n.304-124_304-121del
XM_011515468.3:c.304-124_304-121del	XP_011513770.1:n.304-124_304-121del
NM_203288.2:c.406-124_406-121del MANE Select	NP_976033.1:n.406-124_406-121del