Canonical Allele Identifier: CA2774965027

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096671_33096672insA , CM000669.2:g.33096671_33096672insA	GRCh38
NC_000007.13:g.33136283_33136284insA , CM000669.1:g.33136283_33136284insA	GRCh37
NC_000007.12:g.33102808_33102809insA	NCBI36
NG_012968.1:g.17719_17720insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-118_2379-117insT
ENST00000492391.2:n.1530-118_1530-117insT
ENST00000682645.1:n.3477-118_3477-117insT
ENST00000683432.1:c.*581-118_*581-117insT	ENSP00000508174.1:n.*581-118_*581-117insT
ENST00000684207.1:c.406-118_406-117insT	ENSP00000506942.1:n.406-118_406-117insT
ENST00000297157.8:c.406-118_406-117insT MANE Select	ENSP00000297157.3:n.406-118_406-117insT
ENST00000297157.7:c.406-118_406-117insT	ENSP00000297157.3:n.406-118_406-117insT
ENST00000448915.1:c.304-118_304-117insT	ENSP00000411577.1:n.304-118_304-117insT
NM_203288.1:c.406-118_406-117insT	NP_976033.1:n.406-118_406-117insT
XM_011515468.1:c.304-118_304-117insT	XP_011513770.1:n.304-118_304-117insT
XM_011515468.3:c.304-118_304-117insT	XP_011513770.1:n.304-118_304-117insT
NM_203288.2:c.406-118_406-117insT MANE Select	NP_976033.1:n.406-118_406-117insT