Canonical Allele Identifier: CA573515882

Gene: RP9

Linked Data

• dbSNP Id: rs1318832766
• gnomAD v2: 7-33136198-AGGC-A
• gnomAD v4: 7-33096586-AGGC-A
• MyVariant Identifiers: chr7:g.33136199_33136201del (hg19) ; chr7:g.33096587_33096589del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096587_33096589del , CM000669.2:g.33096587_33096589del	GRCh38
NC_000007.13:g.33136199_33136201del , CM000669.1:g.33136199_33136201del	GRCh37
NC_000007.12:g.33102724_33102726del	NCBI36
NG_012968.1:g.17802_17804del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-35_2379-33del
ENST00000492391.2:n.1530-35_1530-33del
ENST00000682645.1:n.3477-35_3477-33del
ENST00000683432.1:c.*581-35_*581-33del	ENSP00000508174.1:n.*581-35_*581-33del
ENST00000684207.1:c.406-35_406-33del	ENSP00000506942.1:n.406-35_406-33del
ENST00000297157.8:c.406-35_406-33del MANE Select	ENSP00000297157.3:n.406-35_406-33del
ENST00000297157.7:c.406-35_406-33del	ENSP00000297157.3:n.406-35_406-33del
ENST00000448915.1:c.304-35_304-33del	ENSP00000411577.1:n.304-35_304-33del
NM_203288.1:c.406-35_406-33del	NP_976033.1:n.406-35_406-33del
XM_011515468.1:c.304-35_304-33del	XP_011513770.1:n.304-35_304-33del
XM_011515468.3:c.304-35_304-33del	XP_011513770.1:n.304-35_304-33del
NM_203288.2:c.406-35_406-33del MANE Select	NP_976033.1:n.406-35_406-33del