Canonical Allele Identifier: CA2682311962

Gene: RP9

Linked Data

• gnomAD v4: 7-33096684-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096684T>A , CM000669.2:g.33096684T>A	GRCh38
NC_000007.13:g.33136296T>A , CM000669.1:g.33136296T>A	GRCh37
NC_000007.12:g.33102821T>A	NCBI36
NG_012968.1:g.17707A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-130A>T
ENST00000492391.2:n.1530-130A>T
ENST00000682645.1:n.3477-130A>T
ENST00000683432.1:c.*581-130A>T	ENSP00000508174.1:n.*581-130A>T
ENST00000684207.1:c.406-130A>T	ENSP00000506942.1:n.406-130A>T
ENST00000297157.8:c.406-130A>T MANE Select	ENSP00000297157.3:n.406-130A>T
ENST00000297157.7:c.406-130A>T	ENSP00000297157.3:n.406-130A>T
ENST00000448915.1:c.304-130A>T	ENSP00000411577.1:n.304-130A>T
NM_203288.1:c.406-130A>T	NP_976033.1:n.406-130A>T
XM_011515468.1:c.304-130A>T	XP_011513770.1:n.304-130A>T
XM_011515468.3:c.304-130A>T	XP_011513770.1:n.304-130A>T
NM_203288.2:c.406-130A>T MANE Select	NP_976033.1:n.406-130A>T