Canonical Allele Identifier: CA2774965048

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096692_33096701del , CM000669.2:g.33096692_33096701del	GRCh38
NC_000007.13:g.33136304_33136313del , CM000669.1:g.33136304_33136313del	GRCh37
NC_000007.12:g.33102829_33102838del	NCBI36
NG_012968.1:g.17690_17699del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-147_2379-138del
ENST00000492391.2:n.1530-147_1530-138del
ENST00000682645.1:n.3477-147_3477-138del
ENST00000683432.1:c.*581-147_*581-138del	ENSP00000508174.1:n.*581-147_*581-138del
ENST00000684207.1:c.406-147_406-138del	ENSP00000506942.1:n.406-147_406-138del
ENST00000297157.8:c.406-147_406-138del MANE Select	ENSP00000297157.3:n.406-147_406-138del
ENST00000297157.7:c.406-147_406-138del	ENSP00000297157.3:n.406-147_406-138del
ENST00000448915.1:c.304-147_304-138del	ENSP00000411577.1:n.304-147_304-138del
NM_203288.1:c.406-147_406-138del	NP_976033.1:n.406-147_406-138del
XM_011515468.1:c.304-147_304-138del	XP_011513770.1:n.304-147_304-138del
XM_011515468.3:c.304-147_304-138del	XP_011513770.1:n.304-147_304-138del
NM_203288.2:c.406-147_406-138del MANE Select	NP_976033.1:n.406-147_406-138del