Canonical Allele Identifier: CA2424844475
Gene: RPGR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38286179_38286206delinsTTCCCCTTCTCCTTCCTCCTCTTCCCCC , CM000685.2:g.38286179_38286206delinsTTCCCCTTCTCCTTCCTCCTCTTCCCCC GRCh38
NC_000023.10:g.38145432_38145459delinsTTCCCCTTCTCCTTCCTCCTCTTCCCCC , CM000685.1:g.38145432_38145459delinsTTCCCCTTCTCCTTCCTCCTCTTCCCCC GRCh37
NC_000023.9:g.38030376_38030403delinsTTCCCCTTCTCCTTCCTCCTCTTCCCCC NCBI36
NG_009553.1:g.46330_46357delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000494707.6:c.953+1659_953+1686delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA
ENST00000642170.1:n.1826+4753_1826+4780delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA
ENST00000642395.2:c.1905+888_1905+915delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA ENSP00000493468.2:n.1905+888_1905+915delinsGGGGGAAGAGGAGGAAGG...
ENST00000642739.1:c.1572+4753_1572+4780delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA ENSP00000493596.1:n.1572+4753_1572+4780delinsGGGGGAAGAGGAGGAA...
ENST00000644238.1:c.1386+4753_1386+4780delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA ENSP00000496728.1:n.1386+4753_1386+4780delinsGGGGGAAGAGGAGGAA...
ENST00000644337.1:c.1719+888_1719+915delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA ENSP00000494557.1:n.1719+888_1719+915delinsGGGGGAAGAGGAGGAAGG...
ENST00000645032.1:c.2793_2820delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA MANE Select ENSP00000495537.1:p.Glu931=
ENST00000645124.1:c.*101+888_*101+915delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA ENSP00000496446.1:n.*101+888_*101+915delinsGGGGGAAGAGGAGGAAGG...
ENST00000646020.1:c.*594+888_*594+915delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA ENSP00000494745.1:n.*594+888_*594+915delinsGGGGGAAGAGGAGGAAGG...
ENST00000318842.11:c.1905+888_1905+915delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA ENSP00000322219.6:n.1905+888_1905+915delinsGGGGGAAGAGGAGGAAGG...
ENST00000339363.7:c.2520+888_2520+915delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA ENSP00000343671.3:n.2520+888_2520+915delinsGGGGGAAGAGGAGGAAGG...
ENST00000378505.6:c.2793_2820delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA ENSP00000367766.2:p.Glu931=
ENST00000465127.1:c.172-379942_172-379915delinsTTCCCCTTCTCCTTCCTCCTCTTCCCCC ENSP00000417050.1:n.172-379942_172-379915delinsTTCCCCTTCTCCTT...
ENST00000474584.5:c.*37+4753_*37+4780delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA ENSP00000418926.1:n.*37+4753_*37+4780delinsGGGGGAAGAGGAGGAAGG...
ENST00000482855.5:c.1905+888_1905+915delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA ENSP00000419276.1:n.1905+888_1905+915delinsGGGGGAAGAGGAGGAAGG...
ENST00000494707.5:c.139+4753_139+4780delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA
NM_000328.2:c.1905+888_1905+915delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA NP_000319.1:n.1905+888_1905+915delinsGGGGGAAGAGGAGGAAGGAGAAGG...
NM_001034853.1:c.2793_2820delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA NP_001030025.1:p.Glu931=
XM_005272633.1:c.1572+4753_1572+4780delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA XP_005272690.1:n.1572+4753_1572+4780delinsGGGGGAAGAGGAGGAAGGA...
XM_011543940.1:c.1902+888_1902+915delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA XP_011542242.1:n.1902+888_1902+915delinsGGGGGAAGAGGAGGAAGGAGA...
XM_005272633.3:c.1572+4753_1572+4780delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA XP_005272690.1:n.1572+4753_1572+4780delinsGGGGGAAGAGGAGGAAGGA...
XM_011543940.3:c.1902+888_1902+915delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA XP_011542242.1:n.1902+888_1902+915delinsGGGGGAAGAGGAGGAAGGAGA...
XM_017029712.2:c.1569+4753_1569+4780delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA XP_016885201.1:n.1569+4753_1569+4780delinsGGGGGAAGAGGAGGAAGGA...
NM_001367245.1:c.1902+888_1902+915delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA NP_001354174.1:n.1902+888_1902+915delinsGGGGGAAGAGGAGGAAGGAGA...
NM_001367246.1:c.1719+888_1719+915delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA NP_001354175.1:n.1719+888_1719+915delinsGGGGGAAGAGGAGGAAGGAGA...
NM_001367247.1:c.1572+4753_1572+4780delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA NP_001354176.1:n.1572+4753_1572+4780delinsGGGGGAAGAGGAGGAAGGA...
NM_001367248.1:c.1602+4753_1602+4780delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA NP_001354177.1:n.1602+4753_1602+4780delinsGGGGGAAGAGGAGGAAGGA...
NM_001367249.1:c.1569+4753_1569+4780delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA NP_001354178.1:n.1569+4753_1569+4780delinsGGGGGAAGAGGAGGAAGGA...
NM_001367250.1:c.1569+4753_1569+4780delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA NP_001354179.1:n.1569+4753_1569+4780delinsGGGGGAAGAGGAGGAAGGA...
NM_001367251.1:c.1386+4753_1386+4780delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA NP_001354180.1:n.1386+4753_1386+4780delinsGGGGGAAGAGGAGGAAGGA...
NR_159803.1:n.2263+888_2263+915delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA
NR_159804.1:n.1648+4753_1648+4780delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA
NR_159805.1:n.1714+4753_1714+4780delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA
NR_159806.1:n.1866+888_1866+915delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA
NR_159807.1:n.1622+4753_1622+4780delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA
NR_159808.1:n.1826+4753_1826+4780delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA
NM_000328.3:c.1905+888_1905+915delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA NP_000319.1:n.1905+888_1905+915delinsGGGGGAAGAGGAGGAAGGAGAAGG...
NM_001034853.2:c.2793_2820delinsGGGGGAAGAGGAGGAAGGAGAAGGGGAA MANE Select NP_001030025.1:p.Glu931=