Canonical Allele Identifier: CA2424844557
Gene: RPGR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38286278_38286305delinsTTCCTCTTCTCCCTCCCCTTCTCCTTCC , CM000685.2:g.38286278_38286305delinsTTCCTCTTCTCCCTCCCCTTCTCCTTCC GRCh38
NC_000023.10:g.38145531_38145558delinsTTCCTCTTCTCCCTCCCCTTCTCCTTCC , CM000685.1:g.38145531_38145558delinsTTCCTCTTCTCCCTCCCCTTCTCCTTCC GRCh37
NC_000023.9:g.38030475_38030502delinsTTCCTCTTCTCCCTCCCCTTCTCCTTCC NCBI36
NG_009553.1:g.46231_46258delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000494707.6:c.953+1560_953+1587delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA
ENST00000642170.1:n.1826+4654_1826+4681delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA
ENST00000642395.2:c.1905+789_1905+816delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA ENSP00000493468.2:n.1905+789_1905+816delinsGGAAGGAGAAGGGGAGGG...
ENST00000642739.1:c.1572+4654_1572+4681delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA ENSP00000493596.1:n.1572+4654_1572+4681delinsGGAAGGAGAAGGGGAG...
ENST00000644238.1:c.1386+4654_1386+4681delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA ENSP00000496728.1:n.1386+4654_1386+4681delinsGGAAGGAGAAGGGGAG...
ENST00000644337.1:c.1719+789_1719+816delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA ENSP00000494557.1:n.1719+789_1719+816delinsGGAAGGAGAAGGGGAGGG...
ENST00000645032.1:c.2694_2721delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA MANE Select ENSP00000495537.1:p.Glu898=
ENST00000645124.1:c.*101+789_*101+816delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA ENSP00000496446.1:n.*101+789_*101+816delinsGGAAGGAGAAGGGGAGGG...
ENST00000646020.1:c.*594+789_*594+816delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA ENSP00000494745.1:n.*594+789_*594+816delinsGGAAGGAGAAGGGGAGGG...
ENST00000318842.11:c.1905+789_1905+816delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA ENSP00000322219.6:n.1905+789_1905+816delinsGGAAGGAGAAGGGGAGGG...
ENST00000339363.7:c.2520+789_2520+816delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA ENSP00000343671.3:n.2520+789_2520+816delinsGGAAGGAGAAGGGGAGGG...
ENST00000378505.6:c.2694_2721delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA ENSP00000367766.2:p.Glu898=
ENST00000465127.1:c.172-379843_172-379816delinsTTCCTCTTCTCCCTCCCCTTCTCCTTCC ENSP00000417050.1:n.172-379843_172-379816delinsTTCCTCTTCTCCCT...
ENST00000474584.5:c.*37+4654_*37+4681delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA ENSP00000418926.1:n.*37+4654_*37+4681delinsGGAAGGAGAAGGGGAGGG...
ENST00000482855.5:c.1905+789_1905+816delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA ENSP00000419276.1:n.1905+789_1905+816delinsGGAAGGAGAAGGGGAGGG...
ENST00000494707.5:c.139+4654_139+4681delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA
NM_000328.2:c.1905+789_1905+816delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA NP_000319.1:n.1905+789_1905+816delinsGGAAGGAGAAGGGGAGGGAGAAGA...
NM_001034853.1:c.2694_2721delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA NP_001030025.1:p.Glu898=
XM_005272633.1:c.1572+4654_1572+4681delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA XP_005272690.1:n.1572+4654_1572+4681delinsGGAAGGAGAAGGGGAGGGA...
XM_011543940.1:c.1902+789_1902+816delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA XP_011542242.1:n.1902+789_1902+816delinsGGAAGGAGAAGGGGAGGGAGA...
XM_005272633.3:c.1572+4654_1572+4681delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA XP_005272690.1:n.1572+4654_1572+4681delinsGGAAGGAGAAGGGGAGGGA...
XM_011543940.3:c.1902+789_1902+816delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA XP_011542242.1:n.1902+789_1902+816delinsGGAAGGAGAAGGGGAGGGAGA...
XM_017029712.2:c.1569+4654_1569+4681delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA XP_016885201.1:n.1569+4654_1569+4681delinsGGAAGGAGAAGGGGAGGGA...
NM_001367245.1:c.1902+789_1902+816delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA NP_001354174.1:n.1902+789_1902+816delinsGGAAGGAGAAGGGGAGGGAGA...
NM_001367246.1:c.1719+789_1719+816delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA NP_001354175.1:n.1719+789_1719+816delinsGGAAGGAGAAGGGGAGGGAGA...
NM_001367247.1:c.1572+4654_1572+4681delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA NP_001354176.1:n.1572+4654_1572+4681delinsGGAAGGAGAAGGGGAGGGA...
NM_001367248.1:c.1602+4654_1602+4681delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA NP_001354177.1:n.1602+4654_1602+4681delinsGGAAGGAGAAGGGGAGGGA...
NM_001367249.1:c.1569+4654_1569+4681delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA NP_001354178.1:n.1569+4654_1569+4681delinsGGAAGGAGAAGGGGAGGGA...
NM_001367250.1:c.1569+4654_1569+4681delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA NP_001354179.1:n.1569+4654_1569+4681delinsGGAAGGAGAAGGGGAGGGA...
NM_001367251.1:c.1386+4654_1386+4681delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA NP_001354180.1:n.1386+4654_1386+4681delinsGGAAGGAGAAGGGGAGGGA...
NR_159803.1:n.2263+789_2263+816delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA
NR_159804.1:n.1648+4654_1648+4681delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA
NR_159805.1:n.1714+4654_1714+4681delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA
NR_159806.1:n.1866+789_1866+816delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA
NR_159807.1:n.1622+4654_1622+4681delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA
NR_159808.1:n.1826+4654_1826+4681delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA
NM_000328.3:c.1905+789_1905+816delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA NP_000319.1:n.1905+789_1905+816delinsGGAAGGAGAAGGGGAGGGAGAAGA...
NM_001034853.2:c.2694_2721delinsGGAAGGAGAAGGGGAGGGAGAAGAGGAA MANE Select NP_001030025.1:p.Glu898=