Canonical Allele Identifier: CA2774964979

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096631_33096632insAG , CM000669.2:g.33096631_33096632insAG	GRCh38
NC_000007.13:g.33136243_33136244insAG , CM000669.1:g.33136243_33136244insAG	GRCh37
NC_000007.12:g.33102768_33102769insAG	NCBI36
NG_012968.1:g.17759_17760insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-78_2379-77insCT
ENST00000492391.2:n.1530-78_1530-77insCT
ENST00000682645.1:n.3477-78_3477-77insCT
ENST00000683432.1:c.*581-78_*581-77insCT	ENSP00000508174.1:n.*581-78_*581-77insCT
ENST00000684207.1:c.406-78_406-77insCT	ENSP00000506942.1:n.406-78_406-77insCT
ENST00000297157.8:c.406-78_406-77insCT MANE Select	ENSP00000297157.3:n.406-78_406-77insCT
ENST00000297157.7:c.406-78_406-77insCT	ENSP00000297157.3:n.406-78_406-77insCT
ENST00000448915.1:c.304-78_304-77insCT	ENSP00000411577.1:n.304-78_304-77insCT
NM_203288.1:c.406-78_406-77insCT	NP_976033.1:n.406-78_406-77insCT
XM_011515468.1:c.304-78_304-77insCT	XP_011513770.1:n.304-78_304-77insCT
XM_011515468.3:c.304-78_304-77insCT	XP_011513770.1:n.304-78_304-77insCT
NM_203288.2:c.406-78_406-77insCT MANE Select	NP_976033.1:n.406-78_406-77insCT