Canonical Allele Identifier: CA1698611607

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096586_33096589delinsAGGC , CM000669.2:g.33096586_33096589delinsAGGC	GRCh38
NC_000007.13:g.33136198_33136201delinsAGGC , CM000669.1:g.33136198_33136201delinsAGGC	GRCh37
NC_000007.12:g.33102723_33102726delinsAGGC	NCBI36
NG_012968.1:g.17802_17805delinsGCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-35_2379-32delinsGCCT
ENST00000492391.2:n.1530-35_1530-32delinsGCCT
ENST00000682645.1:n.3477-35_3477-32delinsGCCT
ENST00000683432.1:c.*581-35_*581-32delinsGCCT	ENSP00000508174.1:n.*581-35_*581-32delinsGCCT
ENST00000684207.1:c.406-35_406-32delinsGCCT	ENSP00000506942.1:n.406-35_406-32delinsGCCT
ENST00000297157.8:c.406-35_406-32delinsGCCT MANE Select	ENSP00000297157.3:n.406-35_406-32delinsGCCT
ENST00000297157.7:c.406-35_406-32delinsGCCT	ENSP00000297157.3:n.406-35_406-32delinsGCCT
ENST00000448915.1:c.304-35_304-32delinsGCCT	ENSP00000411577.1:n.304-35_304-32delinsGCCT
NM_203288.1:c.406-35_406-32delinsGCCT	NP_976033.1:n.406-35_406-32delinsGCCT
XM_011515468.1:c.304-35_304-32delinsGCCT	XP_011513770.1:n.304-35_304-32delinsGCCT
XM_011515468.3:c.304-35_304-32delinsGCCT	XP_011513770.1:n.304-35_304-32delinsGCCT
NM_203288.2:c.406-35_406-32delinsGCCT MANE Select	NP_976033.1:n.406-35_406-32delinsGCCT