Canonical Allele Identifier: CA1698611681

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096772_33096773delinsAC , CM000669.2:g.33096772_33096773delinsAC	GRCh38
NC_000007.13:g.33136384_33136385delinsAC , CM000669.1:g.33136384_33136385delinsAC	GRCh37
NC_000007.12:g.33102909_33102910delinsAC	NCBI36
NG_012968.1:g.17618_17619delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-219_2379-218delinsGT
ENST00000492391.2:n.1530-219_1530-218delinsGT
ENST00000682645.1:n.3477-219_3477-218delinsGT
ENST00000683432.1:c.*581-219_*581-218delinsGT	ENSP00000508174.1:n.*581-219_*581-218delinsGT
ENST00000684207.1:c.406-219_406-218delinsGT	ENSP00000506942.1:n.406-219_406-218delinsGT
ENST00000297157.8:c.406-219_406-218delinsGT MANE Select	ENSP00000297157.3:n.406-219_406-218delinsGT
ENST00000297157.7:c.406-219_406-218delinsGT	ENSP00000297157.3:n.406-219_406-218delinsGT
ENST00000448915.1:c.304-219_304-218delinsGT	ENSP00000411577.1:n.304-219_304-218delinsGT
NM_203288.1:c.406-219_406-218delinsGT	NP_976033.1:n.406-219_406-218delinsGT
XM_011515468.1:c.304-219_304-218delinsGT	XP_011513770.1:n.304-219_304-218delinsGT
XM_011515468.3:c.304-219_304-218delinsGT	XP_011513770.1:n.304-219_304-218delinsGT
NM_203288.2:c.406-219_406-218delinsGT MANE Select	NP_976033.1:n.406-219_406-218delinsGT