Canonical Allele Identifier: CA2424844337
Gene: RPGR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38286034_38286054delinsCCCCTTCTCCTTCCTCCTCTT , CM000685.2:g.38286034_38286054delinsCCCCTTCTCCTTCCTCCTCTT GRCh38
NC_000023.10:g.38145287_38145307delinsCCCCTTCTCCTTCCTCCTCTT , CM000685.1:g.38145287_38145307delinsCCCCTTCTCCTTCCTCCTCTT GRCh37
NC_000023.9:g.38030231_38030251delinsCCCCTTCTCCTTCCTCCTCTT NCBI36
NG_009553.1:g.46482_46502delinsAAGAGGAGGAAGGAGAAGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000494707.6:c.953+1811_953+1831delinsAAGAGGAGGAAGGAGAAGGGG
ENST00000642170.1:n.1826+4905_1826+4925delinsAAGAGGAGGAAGGAGAAGGGG
ENST00000642395.2:c.1905+1040_1905+1060delinsAAGAGGAGGAAGGAGAAGGGG ENSP00000493468.2:n.1905+1040_1905+1060delinsAAGAGGAGGAAGGAGA...
ENST00000642739.1:c.1572+4905_1572+4925delinsAAGAGGAGGAAGGAGAAGGGG ENSP00000493596.1:n.1572+4905_1572+4925delinsAAGAGGAGGAAGGAGA...
ENST00000644238.1:c.1386+4905_1386+4925delinsAAGAGGAGGAAGGAGAAGGGG ENSP00000496728.1:n.1386+4905_1386+4925delinsAAGAGGAGGAAGGAGA...
ENST00000644337.1:c.1719+1040_1719+1060delinsAAGAGGAGGAAGGAGAAGGGG ENSP00000494557.1:n.1719+1040_1719+1060delinsAAGAGGAGGAAGGAGA...
ENST00000645032.1:c.2945_2965delinsAAGAGGAGGAAGGAGAAGGGG MANE Select ENSP00000495537.1:p.Glu982=
ENST00000645124.1:c.*101+1040_*101+1060delinsAAGAGGAGGAAGGAGAAGGGG ENSP00000496446.1:n.*101+1040_*101+1060delinsAAGAGGAGGAAGGAGA...
ENST00000646020.1:c.*594+1040_*594+1060delinsAAGAGGAGGAAGGAGAAGGGG ENSP00000494745.1:n.*594+1040_*594+1060delinsAAGAGGAGGAAGGAGA...
ENST00000318842.11:c.1905+1040_1905+1060delinsAAGAGGAGGAAGGAGAAGGGG ENSP00000322219.6:n.1905+1040_1905+1060delinsAAGAGGAGGAAGGAGA...
ENST00000339363.7:c.2520+1040_2520+1060delinsAAGAGGAGGAAGGAGAAGGGG ENSP00000343671.3:n.2520+1040_2520+1060delinsAAGAGGAGGAAGGAGA...
ENST00000378505.6:c.2945_2965delinsAAGAGGAGGAAGGAGAAGGGG ENSP00000367766.2:p.Glu982=
ENST00000465127.1:c.172-380087_172-380067delinsCCCCTTCTCCTTCCTCCTCTT ENSP00000417050.1:n.172-380087_172-380067delinsCCCCTTCTCCTTCC...
ENST00000474584.5:c.*37+4905_*37+4925delinsAAGAGGAGGAAGGAGAAGGGG ENSP00000418926.1:n.*37+4905_*37+4925delinsAAGAGGAGGAAGGAGAAG...
ENST00000482855.5:c.1905+1040_1905+1060delinsAAGAGGAGGAAGGAGAAGGGG ENSP00000419276.1:n.1905+1040_1905+1060delinsAAGAGGAGGAAGGAGA...
ENST00000494707.5:c.139+4905_139+4925delinsAAGAGGAGGAAGGAGAAGGGG
NM_000328.2:c.1905+1040_1905+1060delinsAAGAGGAGGAAGGAGAAGGGG NP_000319.1:n.1905+1040_1905+1060delinsAAGAGGAGGAAGGAGAAGGGG
NM_001034853.1:c.2945_2965delinsAAGAGGAGGAAGGAGAAGGGG NP_001030025.1:p.Glu982=
XM_005272633.1:c.1572+4905_1572+4925delinsAAGAGGAGGAAGGAGAAGGGG XP_005272690.1:n.1572+4905_1572+4925delinsAAGAGGAGGAAGGAGAAGG...
XM_011543940.1:c.1902+1040_1902+1060delinsAAGAGGAGGAAGGAGAAGGGG XP_011542242.1:n.1902+1040_1902+1060delinsAAGAGGAGGAAGGAGAAGG...
XM_005272633.3:c.1572+4905_1572+4925delinsAAGAGGAGGAAGGAGAAGGGG XP_005272690.1:n.1572+4905_1572+4925delinsAAGAGGAGGAAGGAGAAGG...
XM_011543940.3:c.1902+1040_1902+1060delinsAAGAGGAGGAAGGAGAAGGGG XP_011542242.1:n.1902+1040_1902+1060delinsAAGAGGAGGAAGGAGAAGG...
XM_017029712.2:c.1569+4905_1569+4925delinsAAGAGGAGGAAGGAGAAGGGG XP_016885201.1:n.1569+4905_1569+4925delinsAAGAGGAGGAAGGAGAAGG...
NM_001367245.1:c.1902+1040_1902+1060delinsAAGAGGAGGAAGGAGAAGGGG NP_001354174.1:n.1902+1040_1902+1060delinsAAGAGGAGGAAGGAGAAGG...
NM_001367246.1:c.1719+1040_1719+1060delinsAAGAGGAGGAAGGAGAAGGGG NP_001354175.1:n.1719+1040_1719+1060delinsAAGAGGAGGAAGGAGAAGG...
NM_001367247.1:c.1572+4905_1572+4925delinsAAGAGGAGGAAGGAGAAGGGG NP_001354176.1:n.1572+4905_1572+4925delinsAAGAGGAGGAAGGAGAAGG...
NM_001367248.1:c.1602+4905_1602+4925delinsAAGAGGAGGAAGGAGAAGGGG NP_001354177.1:n.1602+4905_1602+4925delinsAAGAGGAGGAAGGAGAAGG...
NM_001367249.1:c.1569+4905_1569+4925delinsAAGAGGAGGAAGGAGAAGGGG NP_001354178.1:n.1569+4905_1569+4925delinsAAGAGGAGGAAGGAGAAGG...
NM_001367250.1:c.1569+4905_1569+4925delinsAAGAGGAGGAAGGAGAAGGGG NP_001354179.1:n.1569+4905_1569+4925delinsAAGAGGAGGAAGGAGAAGG...
NM_001367251.1:c.1386+4905_1386+4925delinsAAGAGGAGGAAGGAGAAGGGG NP_001354180.1:n.1386+4905_1386+4925delinsAAGAGGAGGAAGGAGAAGG...
NR_159803.1:n.2263+1040_2263+1060delinsAAGAGGAGGAAGGAGAAGGGG
NR_159804.1:n.1648+4905_1648+4925delinsAAGAGGAGGAAGGAGAAGGGG
NR_159805.1:n.1714+4905_1714+4925delinsAAGAGGAGGAAGGAGAAGGGG
NR_159806.1:n.1866+1040_1866+1060delinsAAGAGGAGGAAGGAGAAGGGG
NR_159807.1:n.1622+4905_1622+4925delinsAAGAGGAGGAAGGAGAAGGGG
NR_159808.1:n.1826+4905_1826+4925delinsAAGAGGAGGAAGGAGAAGGGG
NM_000328.3:c.1905+1040_1905+1060delinsAAGAGGAGGAAGGAGAAGGGG NP_000319.1:n.1905+1040_1905+1060delinsAAGAGGAGGAAGGAGAAGGGG
NM_001034853.2:c.2945_2965delinsAAGAGGAGGAAGGAGAAGGGG MANE Select NP_001030025.1:p.Glu982=