Canonical Allele Identifier: CA2424844858
Gene: RPGR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38286644_38286672delinsCTCCTCCTTCCCCGCTCTTTCCTCCTTTT , CM000685.2:g.38286644_38286672delinsCTCCTCCTTCCCCGCTCTTTCCTCCTTTT GRCh38
NC_000023.10:g.38145897_38145925delinsCTCCTCCTTCCCCGCTCTTTCCTCCTTTT , CM000685.1:g.38145897_38145925delinsCTCCTCCTTCCCCGCTCTTTCCTCCTTTT GRCh37
NC_000023.9:g.38030841_38030869delinsCTCCTCCTTCCCCGCTCTTTCCTCCTTTT NCBI36
NG_009553.1:g.45864_45892delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG

Transcript Alleles

HGVS Amino-acid change
ENST00000494707.6:c.953+1193_953+1221delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG
ENST00000642170.1:n.1826+4287_1826+4315delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG
ENST00000642395.2:c.1905+422_1905+450delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG ENSP00000493468.2:n.1905+422_1905+450deli...
ENST00000642739.1:c.1572+4287_1572+4315delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG ENSP00000493596.1:n.1572+4287_1572+4315de...
ENST00000644238.1:c.1386+4287_1386+4315delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG ENSP00000496728.1:n.1386+4287_1386+4315de...
ENST00000644337.1:c.1719+422_1719+450delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG ENSP00000494557.1:n.1719+422_1719+450deli...
ENST00000645032.1:c.2327_2355delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG MANE Select ENSP00000495537.1:p.Lys776=
ENST00000645124.1:c.*101+422_*101+450delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG ENSP00000496446.1:n.*101+422_*101+450deli...
ENST00000646020.1:c.*594+422_*594+450delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG ENSP00000494745.1:n.*594+422_*594+450deli...
ENST00000318842.11:c.1905+422_1905+450delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG ENSP00000322219.6:n.1905+422_1905+450deli...
ENST00000339363.7:c.2520+422_2520+450delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG ENSP00000343671.3:n.2520+422_2520+450deli...
ENST00000378505.6:c.2327_2355delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG ENSP00000367766.2:p.Lys776=
ENST00000465127.1:c.172-379477_172-379449delinsCTCCTCCTTCCCCGCTCTTTCCTCCTTTT ENSP00000417050.1:n.172-379477_172-379449...
ENST00000474584.5:c.*37+4287_*37+4315delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG ENSP00000418926.1:n.*37+4287_*37+4315deli...
ENST00000482855.5:c.1905+422_1905+450delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG ENSP00000419276.1:n.1905+422_1905+450deli...
ENST00000494707.5:c.139+4287_139+4315delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG
NM_000328.2:c.1905+422_1905+450delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG NP_000319.1:n.1905+422_1905+450delinsAAAA...
NM_001034853.1:c.2327_2355delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG NP_001030025.1:p.Lys776=
XM_005272633.1:c.1572+4287_1572+4315delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG XP_005272690.1:n.1572+4287_1572+4315delin...
XM_011543940.1:c.1902+422_1902+450delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG XP_011542242.1:n.1902+422_1902+450delinsA...
XM_005272633.3:c.1572+4287_1572+4315delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG XP_005272690.1:n.1572+4287_1572+4315delin...
XM_011543940.3:c.1902+422_1902+450delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG XP_011542242.1:n.1902+422_1902+450delinsA...
XM_017029712.2:c.1569+4287_1569+4315delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG XP_016885201.1:n.1569+4287_1569+4315delin...
NM_001367245.1:c.1902+422_1902+450delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG NP_001354174.1:n.1902+422_1902+450delinsA...
NM_001367246.1:c.1719+422_1719+450delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG NP_001354175.1:n.1719+422_1719+450delinsA...
NM_001367247.1:c.1572+4287_1572+4315delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG NP_001354176.1:n.1572+4287_1572+4315delin...
NM_001367248.1:c.1602+4287_1602+4315delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG NP_001354177.1:n.1602+4287_1602+4315delin...
NM_001367249.1:c.1569+4287_1569+4315delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG NP_001354178.1:n.1569+4287_1569+4315delin...
NM_001367250.1:c.1569+4287_1569+4315delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG NP_001354179.1:n.1569+4287_1569+4315delin...
NM_001367251.1:c.1386+4287_1386+4315delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG NP_001354180.1:n.1386+4287_1386+4315delin...
NR_159803.1:n.2263+422_2263+450delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG
NR_159804.1:n.1648+4287_1648+4315delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG
NR_159805.1:n.1714+4287_1714+4315delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG
NR_159806.1:n.1866+422_1866+450delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG
NR_159807.1:n.1622+4287_1622+4315delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG
NR_159808.1:n.1826+4287_1826+4315delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG
NM_000328.3:c.1905+422_1905+450delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG NP_000319.1:n.1905+422_1905+450delinsAAAA...
NM_001034853.2:c.2327_2355delinsAAAAGGAGGAAAGAGCGGGGAAGGAGGAG MANE Select NP_001030025.1:p.Lys776=