Canonical Allele Identifier: CA2774964966

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096627_33096629del , CM000669.2:g.33096627_33096629del	GRCh38
NC_000007.13:g.33136239_33136241del , CM000669.1:g.33136239_33136241del	GRCh37
NC_000007.12:g.33102764_33102766del	NCBI36
NG_012968.1:g.17763_17765del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-74_2379-72del
ENST00000492391.2:n.1530-74_1530-72del
ENST00000682645.1:n.3477-74_3477-72del
ENST00000683432.1:c.*581-74_*581-72del	ENSP00000508174.1:n.*581-74_*581-72del
ENST00000684207.1:c.406-74_406-72del	ENSP00000506942.1:n.406-74_406-72del
ENST00000297157.8:c.406-74_406-72del MANE Select	ENSP00000297157.3:n.406-74_406-72del
ENST00000297157.7:c.406-74_406-72del	ENSP00000297157.3:n.406-74_406-72del
ENST00000448915.1:c.304-74_304-72del	ENSP00000411577.1:n.304-74_304-72del
NM_203288.1:c.406-74_406-72del	NP_976033.1:n.406-74_406-72del
XM_011515468.1:c.304-74_304-72del	XP_011513770.1:n.304-74_304-72del
XM_011515468.3:c.304-74_304-72del	XP_011513770.1:n.304-74_304-72del
NM_203288.2:c.406-74_406-72del MANE Select	NP_976033.1:n.406-74_406-72del