Canonical Allele Identifier: CA1698611698

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096816_33096827delinsTATAACACTGCC , CM000669.2:g.33096816_33096827delinsTATAACACTGCC	GRCh38
NC_000007.13:g.33136428_33136439delinsTATAACACTGCC , CM000669.1:g.33136428_33136439delinsTATAACACTGCC	GRCh37
NC_000007.12:g.33102953_33102964delinsTATAACACTGCC	NCBI36
NG_012968.1:g.17564_17575delinsGGCAGTGTTATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-273_2379-262delinsGGCAGTGTTATA
ENST00000492391.2:n.1530-273_1530-262delinsGGCAGTGTTATA
ENST00000682645.1:n.3477-273_3477-262delinsGGCAGTGTTATA
ENST00000683432.1:c.*581-273_*581-262delinsGGCAGTGTTATA	ENSP00000508174.1:n.*581-273_*581-262delinsGGCAGTGTTATA
ENST00000684207.1:c.406-273_406-262delinsGGCAGTGTTATA	ENSP00000506942.1:n.406-273_406-262delinsGGCAGTGTTATA
ENST00000297157.8:c.406-273_406-262delinsGGCAGTGTTATA MANE Select	ENSP00000297157.3:n.406-273_406-262delinsGGCAGTGTTATA
ENST00000297157.7:c.406-273_406-262delinsGGCAGTGTTATA	ENSP00000297157.3:n.406-273_406-262delinsGGCAGTGTTATA
ENST00000448915.1:c.304-273_304-262delinsGGCAGTGTTATA	ENSP00000411577.1:n.304-273_304-262delinsGGCAGTGTTATA
NM_203288.1:c.406-273_406-262delinsGGCAGTGTTATA	NP_976033.1:n.406-273_406-262delinsGGCAGTGTTATA
XM_011515468.1:c.304-273_304-262delinsGGCAGTGTTATA	XP_011513770.1:n.304-273_304-262delinsGGCAGTGTTATA
XM_011515468.3:c.304-273_304-262delinsGGCAGTGTTATA	XP_011513770.1:n.304-273_304-262delinsGGCAGTGTTATA
NM_203288.2:c.406-273_406-262delinsGGCAGTGTTATA MANE Select	NP_976033.1:n.406-273_406-262delinsGGCAGTGTTATA