Canonical Allele Identifier: CA2682311841

Gene: RP9

Linked Data

• gnomAD v4: 7-33096427-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096431dup , CM000669.2:g.33096431dup	GRCh38
NC_000007.13:g.33136043dup , CM000669.1:g.33136043dup	GRCh37
NC_000007.12:g.33102568dup	NCBI36
NG_012968.1:g.17963dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2440+65dup
ENST00000492391.2:n.1591+65dup
ENST00000682645.1:n.3538+65dup
ENST00000683432.1:c.*642+65dup	ENSP00000508174.1:n.*642+65dup
ENST00000684207.1:c.*61dup	ENSP00000506942.1:n.*61dup
ENST00000297157.8:c.467+65dup MANE Select	ENSP00000297157.3:n.467+65dup
ENST00000297157.7:c.467+65dup	ENSP00000297157.3:n.467+65dup
ENST00000448915.1:c.365+65dup	ENSP00000411577.1:n.365+65dup
NM_203288.1:c.467+65dup	NP_976033.1:n.467+65dup
XM_011515468.1:c.365+65dup	XP_011513770.1:n.365+65dup
XM_011515468.3:c.365+65dup	XP_011513770.1:n.365+65dup
NM_203288.2:c.467+65dup MANE Select	NP_976033.1:n.467+65dup