Canonical Allele Identifier: CA2774964988

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096642_33096643insACA , CM000669.2:g.33096642_33096643insACA	GRCh38
NC_000007.13:g.33136254_33136255insACA , CM000669.1:g.33136254_33136255insACA	GRCh37
NC_000007.12:g.33102779_33102780insACA	NCBI36
NG_012968.1:g.17748_17749insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-89_2379-88insTGT
ENST00000492391.2:n.1530-89_1530-88insTGT
ENST00000682645.1:n.3477-89_3477-88insTGT
ENST00000683432.1:c.*581-89_*581-88insTGT	ENSP00000508174.1:n.*581-89_*581-88insTGT
ENST00000684207.1:c.406-89_406-88insTGT	ENSP00000506942.1:n.406-89_406-88insTGT
ENST00000297157.8:c.406-89_406-88insTGT MANE Select	ENSP00000297157.3:n.406-89_406-88insTGT
ENST00000297157.7:c.406-89_406-88insTGT	ENSP00000297157.3:n.406-89_406-88insTGT
ENST00000448915.1:c.304-89_304-88insTGT	ENSP00000411577.1:n.304-89_304-88insTGT
NM_203288.1:c.406-89_406-88insTGT	NP_976033.1:n.406-89_406-88insTGT
XM_011515468.1:c.304-89_304-88insTGT	XP_011513770.1:n.304-89_304-88insTGT
XM_011515468.3:c.304-89_304-88insTGT	XP_011513770.1:n.304-89_304-88insTGT
NM_203288.2:c.406-89_406-88insTGT MANE Select	NP_976033.1:n.406-89_406-88insTGT