Canonical Allele Identifier: CA2774964968

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096626_33096627insAC , CM000669.2:g.33096626_33096627insAC	GRCh38
NC_000007.13:g.33136238_33136239insAC , CM000669.1:g.33136238_33136239insAC	GRCh37
NC_000007.12:g.33102763_33102764insAC	NCBI36
NG_012968.1:g.17764_17765insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-73_2379-72insGT
ENST00000492391.2:n.1530-73_1530-72insGT
ENST00000682645.1:n.3477-73_3477-72insGT
ENST00000683432.1:c.*581-73_*581-72insGT	ENSP00000508174.1:n.*581-73_*581-72insGT
ENST00000684207.1:c.406-73_406-72insGT	ENSP00000506942.1:n.406-73_406-72insGT
ENST00000297157.8:c.406-73_406-72insGT MANE Select	ENSP00000297157.3:n.406-73_406-72insGT
ENST00000297157.7:c.406-73_406-72insGT	ENSP00000297157.3:n.406-73_406-72insGT
ENST00000448915.1:c.304-73_304-72insGT	ENSP00000411577.1:n.304-73_304-72insGT
NM_203288.1:c.406-73_406-72insGT	NP_976033.1:n.406-73_406-72insGT
XM_011515468.1:c.304-73_304-72insGT	XP_011513770.1:n.304-73_304-72insGT
XM_011515468.3:c.304-73_304-72insGT	XP_011513770.1:n.304-73_304-72insGT
NM_203288.2:c.406-73_406-72insGT MANE Select	NP_976033.1:n.406-73_406-72insGT