Canonical Allele Identifier: CA16621886
Gene: RPGR HGNC NCBI

Linked Data

ClinVar Variation Id: 425488
dbSNP Id: rs1064797364

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38286112del , CM000685.2:g.38286112del GRCh38
NC_000023.10:g.38145365del , CM000685.1:g.38145365del GRCh37
NC_000023.9:g.38030309del NCBI36
NG_009553.1:g.46424del

Transcript Alleles

HGVS Amino-acid change
ENST00000494707.6:c.953+1753del
ENST00000642170.1:n.1826+4847del
ENST00000642395.2:c.1905+982del ENSP00000493468.2:n.1905+982del
ENST00000642739.1:c.1572+4847del ENSP00000493596.1:n.1572+4847del
ENST00000644238.1:c.1386+4847del ENSP00000496728.1:n.1386+4847del
ENST00000644337.1:c.1719+982del ENSP00000494557.1:n.1719+982del
ENST00000645032.1:c.2887del MANE Select ENSP00000495537.1:p.Glu963LysfsTer?
ENST00000645124.1:c.*101+982del ENSP00000496446.1:n.*101+982del
ENST00000646020.1:c.*594+982del ENSP00000494745.1:n.*594+982del
ENST00000318842.11:c.1905+982del ENSP00000322219.6:n.1905+982del
ENST00000339363.7:c.2520+982del ENSP00000343671.3:n.2520+982del
ENST00000378505.6:c.2887del ENSP00000367766.2:p.Glu963LysfsTer?
ENST00000465127.1:c.172-380009del ENSP00000417050.1:n.172-380009del
ENST00000474584.5:c.*37+4847del ENSP00000418926.1:n.*37+4847del
ENST00000482855.5:c.1905+982del ENSP00000419276.1:n.1905+982del
ENST00000494707.5:c.139+4847del
NM_000328.2:c.1905+982del NP_000319.1:n.1905+982del
NM_001034853.1:c.2887del NP_001030025.1:p.Glu963LysfsTer?
XM_005272633.1:c.1572+4847del XP_005272690.1:n.1572+4847del
XM_011543940.1:c.1902+982del XP_011542242.1:n.1902+982del
XM_005272633.3:c.1572+4847del XP_005272690.1:n.1572+4847del
XM_011543940.3:c.1902+982del XP_011542242.1:n.1902+982del
XM_017029712.2:c.1569+4847del XP_016885201.1:n.1569+4847del
NM_001367245.1:c.1902+982del NP_001354174.1:n.1902+982del
NM_001367246.1:c.1719+982del NP_001354175.1:n.1719+982del
NM_001367247.1:c.1572+4847del NP_001354176.1:n.1572+4847del
NM_001367248.1:c.1602+4847del NP_001354177.1:n.1602+4847del
NM_001367249.1:c.1569+4847del NP_001354178.1:n.1569+4847del
NM_001367250.1:c.1569+4847del NP_001354179.1:n.1569+4847del
NM_001367251.1:c.1386+4847del NP_001354180.1:n.1386+4847del
NR_159803.1:n.2263+982del
NR_159804.1:n.1648+4847del
NR_159805.1:n.1714+4847del
NR_159806.1:n.1866+982del
NR_159807.1:n.1622+4847del
NR_159808.1:n.1826+4847del
NM_000328.3:c.1905+982del NP_000319.1:n.1905+982del
NM_001034853.2:c.2887del MANE Select NP_001030025.1:p.Glu963LysfsTer?