Canonical Allele Identifier: CA2774965023

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096668_33096669insCAC , CM000669.2:g.33096668_33096669insCAC	GRCh38
NC_000007.13:g.33136280_33136281insCAC , CM000669.1:g.33136280_33136281insCAC	GRCh37
NC_000007.12:g.33102805_33102806insCAC	NCBI36
NG_012968.1:g.17722_17723insGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-115_2379-114insGTG
ENST00000492391.2:n.1530-115_1530-114insGTG
ENST00000682645.1:n.3477-115_3477-114insGTG
ENST00000683432.1:c.*581-115_*581-114insGTG	ENSP00000508174.1:n.*581-115_*581-114insGTG
ENST00000684207.1:c.406-115_406-114insGTG	ENSP00000506942.1:n.406-115_406-114insGTG
ENST00000297157.8:c.406-115_406-114insGTG MANE Select	ENSP00000297157.3:n.406-115_406-114insGTG
ENST00000297157.7:c.406-115_406-114insGTG	ENSP00000297157.3:n.406-115_406-114insGTG
ENST00000448915.1:c.304-115_304-114insGTG	ENSP00000411577.1:n.304-115_304-114insGTG
NM_203288.1:c.406-115_406-114insGTG	NP_976033.1:n.406-115_406-114insGTG
XM_011515468.1:c.304-115_304-114insGTG	XP_011513770.1:n.304-115_304-114insGTG
XM_011515468.3:c.304-115_304-114insGTG	XP_011513770.1:n.304-115_304-114insGTG
NM_203288.2:c.406-115_406-114insGTG MANE Select	NP_976033.1:n.406-115_406-114insGTG