Canonical Allele Identifier: CA2774965091

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096759_33096760insACA , CM000669.2:g.33096759_33096760insACA	GRCh38
NC_000007.13:g.33136371_33136372insACA , CM000669.1:g.33136371_33136372insACA	GRCh37
NC_000007.12:g.33102896_33102897insACA	NCBI36
NG_012968.1:g.17631_17632insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-206_2379-205insTGT
ENST00000492391.2:n.1530-206_1530-205insTGT
ENST00000682645.1:n.3477-206_3477-205insTGT
ENST00000683432.1:c.*581-206_*581-205insTGT	ENSP00000508174.1:n.*581-206_*581-205insTGT
ENST00000684207.1:c.406-206_406-205insTGT	ENSP00000506942.1:n.406-206_406-205insTGT
ENST00000297157.8:c.406-206_406-205insTGT MANE Select	ENSP00000297157.3:n.406-206_406-205insTGT
ENST00000297157.7:c.406-206_406-205insTGT	ENSP00000297157.3:n.406-206_406-205insTGT
ENST00000448915.1:c.304-206_304-205insTGT	ENSP00000411577.1:n.304-206_304-205insTGT
NM_203288.1:c.406-206_406-205insTGT	NP_976033.1:n.406-206_406-205insTGT
XM_011515468.1:c.304-206_304-205insTGT	XP_011513770.1:n.304-206_304-205insTGT
XM_011515468.3:c.304-206_304-205insTGT	XP_011513770.1:n.304-206_304-205insTGT
NM_203288.2:c.406-206_406-205insTGT MANE Select	NP_976033.1:n.406-206_406-205insTGT