Canonical Allele Identifier: CA2774965089

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096759_33096760del , CM000669.2:g.33096759_33096760del	GRCh38
NC_000007.13:g.33136371_33136372del , CM000669.1:g.33136371_33136372del	GRCh37
NC_000007.12:g.33102896_33102897del	NCBI36
NG_012968.1:g.17631_17632del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-206_2379-205del
ENST00000492391.2:n.1530-206_1530-205del
ENST00000682645.1:n.3477-206_3477-205del
ENST00000683432.1:c.*581-206_*581-205del	ENSP00000508174.1:n.*581-206_*581-205del
ENST00000684207.1:c.406-206_406-205del	ENSP00000506942.1:n.406-206_406-205del
ENST00000297157.8:c.406-206_406-205del MANE Select	ENSP00000297157.3:n.406-206_406-205del
ENST00000297157.7:c.406-206_406-205del	ENSP00000297157.3:n.406-206_406-205del
ENST00000448915.1:c.304-206_304-205del	ENSP00000411577.1:n.304-206_304-205del
NM_203288.1:c.406-206_406-205del	NP_976033.1:n.406-206_406-205del
XM_011515468.1:c.304-206_304-205del	XP_011513770.1:n.304-206_304-205del
XM_011515468.3:c.304-206_304-205del	XP_011513770.1:n.304-206_304-205del
NM_203288.2:c.406-206_406-205del MANE Select	NP_976033.1:n.406-206_406-205del