Canonical Allele Identifier: CA1100004518

Gene: RP9

Linked Data

• dbSNP Id: rs201977708
• gnomAD v3: 7-33096644-A-ATT
• gnomAD v4: 7-33096644-A-ATT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096654_33096655dup , CM000669.2:g.33096654_33096655dup	GRCh38
NC_000007.13:g.33136266_33136267dup , CM000669.1:g.33136266_33136267dup	GRCh37
NC_000007.12:g.33102791_33102792dup	NCBI36
NG_012968.1:g.17745_17746dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-92_2379-91dup
ENST00000492391.2:n.1530-92_1530-91dup
ENST00000682645.1:n.3477-92_3477-91dup
ENST00000683432.1:c.*581-92_*581-91dup	ENSP00000508174.1:n.*581-92_*581-91dup
ENST00000684207.1:c.406-92_406-91dup	ENSP00000506942.1:n.406-92_406-91dup
ENST00000297157.8:c.406-92_406-91dup MANE Select	ENSP00000297157.3:n.406-92_406-91dup
ENST00000297157.7:c.406-92_406-91dup	ENSP00000297157.3:n.406-92_406-91dup
ENST00000448915.1:c.304-92_304-91dup	ENSP00000411577.1:n.304-92_304-91dup
NM_203288.1:c.406-92_406-91dup	NP_976033.1:n.406-92_406-91dup
XM_011515468.1:c.304-92_304-91dup	XP_011513770.1:n.304-92_304-91dup
XM_011515468.3:c.304-92_304-91dup	XP_011513770.1:n.304-92_304-91dup
NM_203288.2:c.406-92_406-91dup MANE Select	NP_976033.1:n.406-92_406-91dup