Canonical Allele Identifier: CA2774965029

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096672_33096673insAGT , CM000669.2:g.33096672_33096673insAGT	GRCh38
NC_000007.13:g.33136284_33136285insAGT , CM000669.1:g.33136284_33136285insAGT	GRCh37
NC_000007.12:g.33102809_33102810insAGT	NCBI36
NG_012968.1:g.17718_17719insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-119_2379-118insACT
ENST00000492391.2:n.1530-119_1530-118insACT
ENST00000682645.1:n.3477-119_3477-118insACT
ENST00000683432.1:c.*581-119_*581-118insACT	ENSP00000508174.1:n.*581-119_*581-118insACT
ENST00000684207.1:c.406-119_406-118insACT	ENSP00000506942.1:n.406-119_406-118insACT
ENST00000297157.8:c.406-119_406-118insACT MANE Select	ENSP00000297157.3:n.406-119_406-118insACT
ENST00000297157.7:c.406-119_406-118insACT	ENSP00000297157.3:n.406-119_406-118insACT
ENST00000448915.1:c.304-119_304-118insACT	ENSP00000411577.1:n.304-119_304-118insACT
NM_203288.1:c.406-119_406-118insACT	NP_976033.1:n.406-119_406-118insACT
XM_011515468.1:c.304-119_304-118insACT	XP_011513770.1:n.304-119_304-118insACT
XM_011515468.3:c.304-119_304-118insACT	XP_011513770.1:n.304-119_304-118insACT
NM_203288.2:c.406-119_406-118insACT MANE Select	NP_976033.1:n.406-119_406-118insACT