Canonical Allele Identifier: CA2774965016

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096664_33096665insCAG , CM000669.2:g.33096664_33096665insCAG	GRCh38
NC_000007.13:g.33136276_33136277insCAG , CM000669.1:g.33136276_33136277insCAG	GRCh37
NC_000007.12:g.33102801_33102802insCAG	NCBI36
NG_012968.1:g.17726_17727insCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-111_2379-110insCTG
ENST00000492391.2:n.1530-111_1530-110insCTG
ENST00000682645.1:n.3477-111_3477-110insCTG
ENST00000683432.1:c.*581-111_*581-110insCTG	ENSP00000508174.1:n.*581-111_*581-110insCTG
ENST00000684207.1:c.406-111_406-110insCTG	ENSP00000506942.1:n.406-111_406-110insCTG
ENST00000297157.8:c.406-111_406-110insCTG MANE Select	ENSP00000297157.3:n.406-111_406-110insCTG
ENST00000297157.7:c.406-111_406-110insCTG	ENSP00000297157.3:n.406-111_406-110insCTG
ENST00000448915.1:c.304-111_304-110insCTG	ENSP00000411577.1:n.304-111_304-110insCTG
NM_203288.1:c.406-111_406-110insCTG	NP_976033.1:n.406-111_406-110insCTG
XM_011515468.1:c.304-111_304-110insCTG	XP_011513770.1:n.304-111_304-110insCTG
XM_011515468.3:c.304-111_304-110insCTG	XP_011513770.1:n.304-111_304-110insCTG
NM_203288.2:c.406-111_406-110insCTG MANE Select	NP_976033.1:n.406-111_406-110insCTG