Canonical Allele Identifier: CA2774965003

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096657_33096658insACA , CM000669.2:g.33096657_33096658insACA	GRCh38
NC_000007.13:g.33136269_33136270insACA , CM000669.1:g.33136269_33136270insACA	GRCh37
NC_000007.12:g.33102794_33102795insACA	NCBI36
NG_012968.1:g.17733_17734insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-104_2379-103insTGT
ENST00000492391.2:n.1530-104_1530-103insTGT
ENST00000682645.1:n.3477-104_3477-103insTGT
ENST00000683432.1:c.*581-104_*581-103insTGT	ENSP00000508174.1:n.*581-104_*581-103insTGT
ENST00000684207.1:c.406-104_406-103insTGT	ENSP00000506942.1:n.406-104_406-103insTGT
ENST00000297157.8:c.406-104_406-103insTGT MANE Select	ENSP00000297157.3:n.406-104_406-103insTGT
ENST00000297157.7:c.406-104_406-103insTGT	ENSP00000297157.3:n.406-104_406-103insTGT
ENST00000448915.1:c.304-104_304-103insTGT	ENSP00000411577.1:n.304-104_304-103insTGT
NM_203288.1:c.406-104_406-103insTGT	NP_976033.1:n.406-104_406-103insTGT
XM_011515468.1:c.304-104_304-103insTGT	XP_011513770.1:n.304-104_304-103insTGT
XM_011515468.3:c.304-104_304-103insTGT	XP_011513770.1:n.304-104_304-103insTGT
NM_203288.2:c.406-104_406-103insTGT MANE Select	NP_976033.1:n.406-104_406-103insTGT