Canonical Allele Identifier: CA2774965060

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096709_33096710insA , CM000669.2:g.33096709_33096710insA	GRCh38
NC_000007.13:g.33136321_33136322insA , CM000669.1:g.33136321_33136322insA	GRCh37
NC_000007.12:g.33102846_33102847insA	NCBI36
NG_012968.1:g.17681_17682insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-156_2379-155insT
ENST00000492391.2:n.1530-156_1530-155insT
ENST00000682645.1:n.3477-156_3477-155insT
ENST00000683432.1:c.*581-156_*581-155insT	ENSP00000508174.1:n.*581-156_*581-155insT
ENST00000684207.1:c.406-156_406-155insT	ENSP00000506942.1:n.406-156_406-155insT
ENST00000297157.8:c.406-156_406-155insT MANE Select	ENSP00000297157.3:n.406-156_406-155insT
ENST00000297157.7:c.406-156_406-155insT	ENSP00000297157.3:n.406-156_406-155insT
ENST00000448915.1:c.304-156_304-155insT	ENSP00000411577.1:n.304-156_304-155insT
NM_203288.1:c.406-156_406-155insT	NP_976033.1:n.406-156_406-155insT
XM_011515468.1:c.304-156_304-155insT	XP_011513770.1:n.304-156_304-155insT
XM_011515468.3:c.304-156_304-155insT	XP_011513770.1:n.304-156_304-155insT
NM_203288.2:c.406-156_406-155insT MANE Select	NP_976033.1:n.406-156_406-155insT