Canonical Allele Identifier: CA2774965081

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096739_33096747del , CM000669.2:g.33096739_33096747del	GRCh38
NC_000007.13:g.33136351_33136359del , CM000669.1:g.33136351_33136359del	GRCh37
NC_000007.12:g.33102876_33102884del	NCBI36
NG_012968.1:g.17647_17655del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-190_2379-182del
ENST00000492391.2:n.1530-190_1530-182del
ENST00000682645.1:n.3477-190_3477-182del
ENST00000683432.1:c.*581-190_*581-182del	ENSP00000508174.1:n.*581-190_*581-182del
ENST00000684207.1:c.406-190_406-182del	ENSP00000506942.1:n.406-190_406-182del
ENST00000297157.8:c.406-190_406-182del MANE Select	ENSP00000297157.3:n.406-190_406-182del
ENST00000297157.7:c.406-190_406-182del	ENSP00000297157.3:n.406-190_406-182del
ENST00000448915.1:c.304-190_304-182del	ENSP00000411577.1:n.304-190_304-182del
NM_203288.1:c.406-190_406-182del	NP_976033.1:n.406-190_406-182del
XM_011515468.1:c.304-190_304-182del	XP_011513770.1:n.304-190_304-182del
XM_011515468.3:c.304-190_304-182del	XP_011513770.1:n.304-190_304-182del
NM_203288.2:c.406-190_406-182del MANE Select	NP_976033.1:n.406-190_406-182del