Canonical Allele Identifier: CA2774965058

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096709_33096714del , CM000669.2:g.33096709_33096714del	GRCh38
NC_000007.13:g.33136321_33136326del , CM000669.1:g.33136321_33136326del	GRCh37
NC_000007.12:g.33102846_33102851del	NCBI36
NG_012968.1:g.17677_17682del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-160_2379-155del
ENST00000492391.2:n.1530-160_1530-155del
ENST00000682645.1:n.3477-160_3477-155del
ENST00000683432.1:c.*581-160_*581-155del	ENSP00000508174.1:n.*581-160_*581-155del
ENST00000684207.1:c.406-160_406-155del	ENSP00000506942.1:n.406-160_406-155del
ENST00000297157.8:c.406-160_406-155del MANE Select	ENSP00000297157.3:n.406-160_406-155del
ENST00000297157.7:c.406-160_406-155del	ENSP00000297157.3:n.406-160_406-155del
ENST00000448915.1:c.304-160_304-155del	ENSP00000411577.1:n.304-160_304-155del
NM_203288.1:c.406-160_406-155del	NP_976033.1:n.406-160_406-155del
XM_011515468.1:c.304-160_304-155del	XP_011513770.1:n.304-160_304-155del
XM_011515468.3:c.304-160_304-155del	XP_011513770.1:n.304-160_304-155del
NM_203288.2:c.406-160_406-155del MANE Select	NP_976033.1:n.406-160_406-155del