Canonical Allele Identifier: CA2774965040

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096681_33096691del , CM000669.2:g.33096681_33096691del	GRCh38
NC_000007.13:g.33136293_33136303del , CM000669.1:g.33136293_33136303del	GRCh37
NC_000007.12:g.33102818_33102828del	NCBI36
NG_012968.1:g.17700_17710del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-137_2379-127del
ENST00000492391.2:n.1530-137_1530-127del
ENST00000682645.1:n.3477-137_3477-127del
ENST00000683432.1:c.*581-137_*581-127del	ENSP00000508174.1:n.*581-137_*581-127del
ENST00000684207.1:c.406-137_406-127del	ENSP00000506942.1:n.406-137_406-127del
ENST00000297157.8:c.406-137_406-127del MANE Select	ENSP00000297157.3:n.406-137_406-127del
ENST00000297157.7:c.406-137_406-127del	ENSP00000297157.3:n.406-137_406-127del
ENST00000448915.1:c.304-137_304-127del	ENSP00000411577.1:n.304-137_304-127del
NM_203288.1:c.406-137_406-127del	NP_976033.1:n.406-137_406-127del
XM_011515468.1:c.304-137_304-127del	XP_011513770.1:n.304-137_304-127del
XM_011515468.3:c.304-137_304-127del	XP_011513770.1:n.304-137_304-127del
NM_203288.2:c.406-137_406-127del MANE Select	NP_976033.1:n.406-137_406-127del