Canonical Allele Identifier: CA2774965084

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096738_33096739insAC , CM000669.2:g.33096738_33096739insAC	GRCh38
NC_000007.13:g.33136350_33136351insAC , CM000669.1:g.33136350_33136351insAC	GRCh37
NC_000007.12:g.33102875_33102876insAC	NCBI36
NG_012968.1:g.17652_17653insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-185_2379-184insGT
ENST00000492391.2:n.1530-185_1530-184insGT
ENST00000682645.1:n.3477-185_3477-184insGT
ENST00000683432.1:c.*581-185_*581-184insGT	ENSP00000508174.1:n.*581-185_*581-184insGT
ENST00000684207.1:c.406-185_406-184insGT	ENSP00000506942.1:n.406-185_406-184insGT
ENST00000297157.8:c.406-185_406-184insGT MANE Select	ENSP00000297157.3:n.406-185_406-184insGT
ENST00000297157.7:c.406-185_406-184insGT	ENSP00000297157.3:n.406-185_406-184insGT
ENST00000448915.1:c.304-185_304-184insGT	ENSP00000411577.1:n.304-185_304-184insGT
NM_203288.1:c.406-185_406-184insGT	NP_976033.1:n.406-185_406-184insGT
XM_011515468.1:c.304-185_304-184insGT	XP_011513770.1:n.304-185_304-184insGT
XM_011515468.3:c.304-185_304-184insGT	XP_011513770.1:n.304-185_304-184insGT
NM_203288.2:c.406-185_406-184insGT MANE Select	NP_976033.1:n.406-185_406-184insGT