Canonical Allele Identifier: CA2774965068

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096716_33096717insAGT , CM000669.2:g.33096716_33096717insAGT	GRCh38
NC_000007.13:g.33136328_33136329insAGT , CM000669.1:g.33136328_33136329insAGT	GRCh37
NC_000007.12:g.33102853_33102854insAGT	NCBI36
NG_012968.1:g.17674_17675insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-163_2379-162insACT
ENST00000492391.2:n.1530-163_1530-162insACT
ENST00000682645.1:n.3477-163_3477-162insACT
ENST00000683432.1:c.*581-163_*581-162insACT	ENSP00000508174.1:n.*581-163_*581-162insACT
ENST00000684207.1:c.406-163_406-162insACT	ENSP00000506942.1:n.406-163_406-162insACT
ENST00000297157.8:c.406-163_406-162insACT MANE Select	ENSP00000297157.3:n.406-163_406-162insACT
ENST00000297157.7:c.406-163_406-162insACT	ENSP00000297157.3:n.406-163_406-162insACT
ENST00000448915.1:c.304-163_304-162insACT	ENSP00000411577.1:n.304-163_304-162insACT
NM_203288.1:c.406-163_406-162insACT	NP_976033.1:n.406-163_406-162insACT
XM_011515468.1:c.304-163_304-162insACT	XP_011513770.1:n.304-163_304-162insACT
XM_011515468.3:c.304-163_304-162insACT	XP_011513770.1:n.304-163_304-162insACT
NM_203288.2:c.406-163_406-162insACT MANE Select	NP_976033.1:n.406-163_406-162insACT