Canonical Allele Identifier: CA2774965065

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096714_33096715insGAG , CM000669.2:g.33096714_33096715insGAG	GRCh38
NC_000007.13:g.33136326_33136327insGAG , CM000669.1:g.33136326_33136327insGAG	GRCh37
NC_000007.12:g.33102851_33102852insGAG	NCBI36
NG_012968.1:g.17676_17677insCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-161_2379-160insCTC
ENST00000492391.2:n.1530-161_1530-160insCTC
ENST00000682645.1:n.3477-161_3477-160insCTC
ENST00000683432.1:c.*581-161_*581-160insCTC	ENSP00000508174.1:n.*581-161_*581-160insCTC
ENST00000684207.1:c.406-161_406-160insCTC	ENSP00000506942.1:n.406-161_406-160insCTC
ENST00000297157.8:c.406-161_406-160insCTC MANE Select	ENSP00000297157.3:n.406-161_406-160insCTC
ENST00000297157.7:c.406-161_406-160insCTC	ENSP00000297157.3:n.406-161_406-160insCTC
ENST00000448915.1:c.304-161_304-160insCTC	ENSP00000411577.1:n.304-161_304-160insCTC
NM_203288.1:c.406-161_406-160insCTC	NP_976033.1:n.406-161_406-160insCTC
XM_011515468.1:c.304-161_304-160insCTC	XP_011513770.1:n.304-161_304-160insCTC
XM_011515468.3:c.304-161_304-160insCTC	XP_011513770.1:n.304-161_304-160insCTC
NM_203288.2:c.406-161_406-160insCTC MANE Select	NP_976033.1:n.406-161_406-160insCTC