Canonical Allele Identifier: CA2595280033

Gene: RP9

Linked Data

• gnomAD v3: 7-33096616-G-GA
• gnomAD v4: 7-33096616-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096619dup , CM000669.2:g.33096619dup	GRCh38
NC_000007.13:g.33136231dup , CM000669.1:g.33136231dup	GRCh37
NC_000007.12:g.33102756dup	NCBI36
NG_012968.1:g.17774dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-63dup
ENST00000492391.2:n.1530-63dup
ENST00000682645.1:n.3477-63dup
ENST00000683432.1:c.*581-63dup	ENSP00000508174.1:n.*581-63dup
ENST00000684207.1:c.406-63dup	ENSP00000506942.1:n.406-63dup
ENST00000297157.8:c.406-63dup MANE Select	ENSP00000297157.3:n.406-63dup
ENST00000297157.7:c.406-63dup	ENSP00000297157.3:n.406-63dup
ENST00000448915.1:c.304-63dup	ENSP00000411577.1:n.304-63dup
NM_203288.1:c.406-63dup	NP_976033.1:n.406-63dup
XM_011515468.1:c.304-63dup	XP_011513770.1:n.304-63dup
XM_011515468.3:c.304-63dup	XP_011513770.1:n.304-63dup
NM_203288.2:c.406-63dup MANE Select	NP_976033.1:n.406-63dup