Canonical Allele Identifier: CA2774965094

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096761_33096762del , CM000669.2:g.33096761_33096762del	GRCh38
NC_000007.13:g.33136373_33136374del , CM000669.1:g.33136373_33136374del	GRCh37
NC_000007.12:g.33102898_33102899del	NCBI36
NG_012968.1:g.17629_17630del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-208_2379-207del
ENST00000492391.2:n.1530-208_1530-207del
ENST00000682645.1:n.3477-208_3477-207del
ENST00000683432.1:c.*581-208_*581-207del	ENSP00000508174.1:n.*581-208_*581-207del
ENST00000684207.1:c.406-208_406-207del	ENSP00000506942.1:n.406-208_406-207del
ENST00000297157.8:c.406-208_406-207del MANE Select	ENSP00000297157.3:n.406-208_406-207del
ENST00000297157.7:c.406-208_406-207del	ENSP00000297157.3:n.406-208_406-207del
ENST00000448915.1:c.304-208_304-207del	ENSP00000411577.1:n.304-208_304-207del
NM_203288.1:c.406-208_406-207del	NP_976033.1:n.406-208_406-207del
XM_011515468.1:c.304-208_304-207del	XP_011513770.1:n.304-208_304-207del
XM_011515468.3:c.304-208_304-207del	XP_011513770.1:n.304-208_304-207del
NM_203288.2:c.406-208_406-207del MANE Select	NP_976033.1:n.406-208_406-207del