Canonical Allele Identifier: CA2774965074

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096718_33096719insAGA , CM000669.2:g.33096718_33096719insAGA	GRCh38
NC_000007.13:g.33136330_33136331insAGA , CM000669.1:g.33136330_33136331insAGA	GRCh37
NC_000007.12:g.33102855_33102856insAGA	NCBI36
NG_012968.1:g.17672_17673insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-165_2379-164insTCT
ENST00000492391.2:n.1530-165_1530-164insTCT
ENST00000682645.1:n.3477-165_3477-164insTCT
ENST00000683432.1:c.*581-165_*581-164insTCT	ENSP00000508174.1:n.*581-165_*581-164insTCT
ENST00000684207.1:c.406-165_406-164insTCT	ENSP00000506942.1:n.406-165_406-164insTCT
ENST00000297157.8:c.406-165_406-164insTCT MANE Select	ENSP00000297157.3:n.406-165_406-164insTCT
ENST00000297157.7:c.406-165_406-164insTCT	ENSP00000297157.3:n.406-165_406-164insTCT
ENST00000448915.1:c.304-165_304-164insTCT	ENSP00000411577.1:n.304-165_304-164insTCT
NM_203288.1:c.406-165_406-164insTCT	NP_976033.1:n.406-165_406-164insTCT
XM_011515468.1:c.304-165_304-164insTCT	XP_011513770.1:n.304-165_304-164insTCT
XM_011515468.3:c.304-165_304-164insTCT	XP_011513770.1:n.304-165_304-164insTCT
NM_203288.2:c.406-165_406-164insTCT MANE Select	NP_976033.1:n.406-165_406-164insTCT