Canonical Allele Identifier: CA2682311925

Gene: RP9

Linked Data

• gnomAD v4: 7-33096644-ATTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096653_33096655del , CM000669.2:g.33096653_33096655del	GRCh38
NC_000007.13:g.33136265_33136267del , CM000669.1:g.33136265_33136267del	GRCh37
NC_000007.12:g.33102790_33102792del	NCBI36
NG_012968.1:g.17744_17746del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-93_2379-91del
ENST00000492391.2:n.1530-93_1530-91del
ENST00000682645.1:n.3477-93_3477-91del
ENST00000683432.1:c.*581-93_*581-91del	ENSP00000508174.1:n.*581-93_*581-91del
ENST00000684207.1:c.406-93_406-91del	ENSP00000506942.1:n.406-93_406-91del
ENST00000297157.8:c.406-93_406-91del MANE Select	ENSP00000297157.3:n.406-93_406-91del
ENST00000297157.7:c.406-93_406-91del	ENSP00000297157.3:n.406-93_406-91del
ENST00000448915.1:c.304-93_304-91del	ENSP00000411577.1:n.304-93_304-91del
NM_203288.1:c.406-93_406-91del	NP_976033.1:n.406-93_406-91del
XM_011515468.1:c.304-93_304-91del	XP_011513770.1:n.304-93_304-91del
XM_011515468.3:c.304-93_304-91del	XP_011513770.1:n.304-93_304-91del
NM_203288.2:c.406-93_406-91del MANE Select	NP_976033.1:n.406-93_406-91del