Canonical Allele Identifier: CA2682311860
Gene: RP9 HGNC NCBI

Linked Data

gnomAD v4: 7-33096462-GGGGATATT-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.33096464_33096471del , CM000669.2:g.33096464_33096471del GRCh38
NC_000007.13:g.33136076_33136083del , CM000669.1:g.33136076_33136083del GRCh37
NC_000007.12:g.33102601_33102608del NCBI36
NG_012968.1:g.17921_17928del

Transcript Alleles

HGVS Amino-acid change
ENST00000474370.2:n.2440+23_2440+30del
ENST00000492391.2:n.1591+23_1591+30del
ENST00000682645.1:n.3538+23_3538+30del
ENST00000683432.1:c.*642+23_*642+30del ENSP00000508174.1:n.*642+23_*642+30del
ENST00000684207.1:c.*19_*26del ENSP00000506942.1:n.*19_*26del
ENST00000297157.8:c.467+23_467+30del MANE Select ENSP00000297157.3:n.467+23_467+30del
ENST00000297157.7:c.467+23_467+30del ENSP00000297157.3:n.467+23_467+30del
ENST00000448915.1:c.365+23_365+30del ENSP00000411577.1:n.365+23_365+30del
NM_203288.1:c.467+23_467+30del NP_976033.1:n.467+23_467+30del
XM_011515468.1:c.365+23_365+30del XP_011513770.1:n.365+23_365+30del
XM_011515468.3:c.365+23_365+30del XP_011513770.1:n.365+23_365+30del
NM_203288.2:c.467+23_467+30del MANE Select NP_976033.1:n.467+23_467+30del
Search 100 bp 5'
Search 100 bp 3'