Canonical Allele Identifier: CA2774964995

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096646_33096647insAGG , CM000669.2:g.33096646_33096647insAGG	GRCh38
NC_000007.13:g.33136258_33136259insAGG , CM000669.1:g.33136258_33136259insAGG	GRCh37
NC_000007.12:g.33102783_33102784insAGG	NCBI36
NG_012968.1:g.17744_17745insCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-93_2379-92insCCT
ENST00000492391.2:n.1530-93_1530-92insCCT
ENST00000682645.1:n.3477-93_3477-92insCCT
ENST00000683432.1:c.*581-93_*581-92insCCT	ENSP00000508174.1:n.*581-93_*581-92insCCT
ENST00000684207.1:c.406-93_406-92insCCT	ENSP00000506942.1:n.406-93_406-92insCCT
ENST00000297157.8:c.406-93_406-92insCCT MANE Select	ENSP00000297157.3:n.406-93_406-92insCCT
ENST00000297157.7:c.406-93_406-92insCCT	ENSP00000297157.3:n.406-93_406-92insCCT
ENST00000448915.1:c.304-93_304-92insCCT	ENSP00000411577.1:n.304-93_304-92insCCT
NM_203288.1:c.406-93_406-92insCCT	NP_976033.1:n.406-93_406-92insCCT
XM_011515468.1:c.304-93_304-92insCCT	XP_011513770.1:n.304-93_304-92insCCT
XM_011515468.3:c.304-93_304-92insCCT	XP_011513770.1:n.304-93_304-92insCCT
NM_203288.2:c.406-93_406-92insCCT MANE Select	NP_976033.1:n.406-93_406-92insCCT