Canonical Allele Identifier: CA2774965008

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096663_33096667del , CM000669.2:g.33096663_33096667del	GRCh38
NC_000007.13:g.33136275_33136279del , CM000669.1:g.33136275_33136279del	GRCh37
NC_000007.12:g.33102800_33102804del	NCBI36
NG_012968.1:g.17725_17729del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-112_2379-108del
ENST00000492391.2:n.1530-112_1530-108del
ENST00000682645.1:n.3477-112_3477-108del
ENST00000683432.1:c.*581-112_*581-108del	ENSP00000508174.1:n.*581-112_*581-108del
ENST00000684207.1:c.406-112_406-108del	ENSP00000506942.1:n.406-112_406-108del
ENST00000297157.8:c.406-112_406-108del MANE Select	ENSP00000297157.3:n.406-112_406-108del
ENST00000297157.7:c.406-112_406-108del	ENSP00000297157.3:n.406-112_406-108del
ENST00000448915.1:c.304-112_304-108del	ENSP00000411577.1:n.304-112_304-108del
NM_203288.1:c.406-112_406-108del	NP_976033.1:n.406-112_406-108del
XM_011515468.1:c.304-112_304-108del	XP_011513770.1:n.304-112_304-108del
XM_011515468.3:c.304-112_304-108del	XP_011513770.1:n.304-112_304-108del
NM_203288.2:c.406-112_406-108del MANE Select	NP_976033.1:n.406-112_406-108del