Canonical Allele Identifier: CA2774965051

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096697_33096698insAGT , CM000669.2:g.33096697_33096698insAGT	GRCh38
NC_000007.13:g.33136309_33136310insAGT , CM000669.1:g.33136309_33136310insAGT	GRCh37
NC_000007.12:g.33102834_33102835insAGT	NCBI36
NG_012968.1:g.17693_17694insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-144_2379-143insACT
ENST00000492391.2:n.1530-144_1530-143insACT
ENST00000682645.1:n.3477-144_3477-143insACT
ENST00000683432.1:c.*581-144_*581-143insACT	ENSP00000508174.1:n.*581-144_*581-143insACT
ENST00000684207.1:c.406-144_406-143insACT	ENSP00000506942.1:n.406-144_406-143insACT
ENST00000297157.8:c.406-144_406-143insACT MANE Select	ENSP00000297157.3:n.406-144_406-143insACT
ENST00000297157.7:c.406-144_406-143insACT	ENSP00000297157.3:n.406-144_406-143insACT
ENST00000448915.1:c.304-144_304-143insACT	ENSP00000411577.1:n.304-144_304-143insACT
NM_203288.1:c.406-144_406-143insACT	NP_976033.1:n.406-144_406-143insACT
XM_011515468.1:c.304-144_304-143insACT	XP_011513770.1:n.304-144_304-143insACT
XM_011515468.3:c.304-144_304-143insACT	XP_011513770.1:n.304-144_304-143insACT
NM_203288.2:c.406-144_406-143insACT MANE Select	NP_976033.1:n.406-144_406-143insACT