Canonical Allele Identifier: CA2774965007

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096660_33096661insACA , CM000669.2:g.33096660_33096661insACA	GRCh38
NC_000007.13:g.33136272_33136273insACA , CM000669.1:g.33136272_33136273insACA	GRCh37
NC_000007.12:g.33102797_33102798insACA	NCBI36
NG_012968.1:g.17730_17731insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-107_2379-106insTGT
ENST00000492391.2:n.1530-107_1530-106insTGT
ENST00000682645.1:n.3477-107_3477-106insTGT
ENST00000683432.1:c.*581-107_*581-106insTGT	ENSP00000508174.1:n.*581-107_*581-106insTGT
ENST00000684207.1:c.406-107_406-106insTGT	ENSP00000506942.1:n.406-107_406-106insTGT
ENST00000297157.8:c.406-107_406-106insTGT MANE Select	ENSP00000297157.3:n.406-107_406-106insTGT
ENST00000297157.7:c.406-107_406-106insTGT	ENSP00000297157.3:n.406-107_406-106insTGT
ENST00000448915.1:c.304-107_304-106insTGT	ENSP00000411577.1:n.304-107_304-106insTGT
NM_203288.1:c.406-107_406-106insTGT	NP_976033.1:n.406-107_406-106insTGT
XM_011515468.1:c.304-107_304-106insTGT	XP_011513770.1:n.304-107_304-106insTGT
XM_011515468.3:c.304-107_304-106insTGT	XP_011513770.1:n.304-107_304-106insTGT
NM_203288.2:c.406-107_406-106insTGT MANE Select	NP_976033.1:n.406-107_406-106insTGT