Canonical Allele Identifier: CA2774965035

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096676_33096677insA , CM000669.2:g.33096676_33096677insA	GRCh38
NC_000007.13:g.33136288_33136289insA , CM000669.1:g.33136288_33136289insA	GRCh37
NC_000007.12:g.33102813_33102814insA	NCBI36
NG_012968.1:g.17714_17715insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-123_2379-122insT
ENST00000492391.2:n.1530-123_1530-122insT
ENST00000682645.1:n.3477-123_3477-122insT
ENST00000683432.1:c.*581-123_*581-122insT	ENSP00000508174.1:n.*581-123_*581-122insT
ENST00000684207.1:c.406-123_406-122insT	ENSP00000506942.1:n.406-123_406-122insT
ENST00000297157.8:c.406-123_406-122insT MANE Select	ENSP00000297157.3:n.406-123_406-122insT
ENST00000297157.7:c.406-123_406-122insT	ENSP00000297157.3:n.406-123_406-122insT
ENST00000448915.1:c.304-123_304-122insT	ENSP00000411577.1:n.304-123_304-122insT
NM_203288.1:c.406-123_406-122insT	NP_976033.1:n.406-123_406-122insT
XM_011515468.1:c.304-123_304-122insT	XP_011513770.1:n.304-123_304-122insT
XM_011515468.3:c.304-123_304-122insT	XP_011513770.1:n.304-123_304-122insT
NM_203288.2:c.406-123_406-122insT MANE Select	NP_976033.1:n.406-123_406-122insT