Canonical Allele Identifier: CA2424844290
Gene: RPGR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38285994_38286015delinsTCTTCCTCCCCTTCTTCTTCCC , CM000685.2:g.38285994_38286015delinsTCTTCCTCCCCTTCTTCTTCCC GRCh38
NC_000023.10:g.38145247_38145268delinsTCTTCCTCCCCTTCTTCTTCCC , CM000685.1:g.38145247_38145268delinsTCTTCCTCCCCTTCTTCTTCCC GRCh37
NC_000023.9:g.38030191_38030212delinsTCTTCCTCCCCTTCTTCTTCCC NCBI36
NG_009553.1:g.46521_46542delinsGGGAAGAAGAAGGGGAGGAAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000494707.6:c.953+1850_953+1871delinsGGGAAGAAGAAGGGGAGGAAGA
ENST00000642170.1:n.1826+4944_1826+4965delinsGGGAAGAAGAAGGGGAGGAAGA
ENST00000642395.2:c.1905+1079_1905+1100delinsGGGAAGAAGAAGGGGAGGAAGA ENSP00000493468.2:n.1905+1079_1905+1100delinsGGGAAGAAGAAGGGGA...
ENST00000642739.1:c.1572+4944_1572+4965delinsGGGAAGAAGAAGGGGAGGAAGA ENSP00000493596.1:n.1572+4944_1572+4965delinsGGGAAGAAGAAGGGGA...
ENST00000644238.1:c.1386+4944_1386+4965delinsGGGAAGAAGAAGGGGAGGAAGA ENSP00000496728.1:n.1386+4944_1386+4965delinsGGGAAGAAGAAGGGGA...
ENST00000644337.1:c.1719+1079_1719+1100delinsGGGAAGAAGAAGGGGAGGAAGA ENSP00000494557.1:n.1719+1079_1719+1100delinsGGGAAGAAGAAGGGGA...
ENST00000645032.1:c.2984_3005delinsGGGAAGAAGAAGGGGAGGAAGA MANE Select ENSP00000495537.1:p.Gly995=
ENST00000645124.1:c.*101+1079_*101+1100delinsGGGAAGAAGAAGGGGAGGAAGA ENSP00000496446.1:n.*101+1079_*101+1100delinsGGGAAGAAGAAGGGGA...
ENST00000646020.1:c.*594+1079_*594+1100delinsGGGAAGAAGAAGGGGAGGAAGA ENSP00000494745.1:n.*594+1079_*594+1100delinsGGGAAGAAGAAGGGGA...
ENST00000318842.11:c.1905+1079_1905+1100delinsGGGAAGAAGAAGGGGAGGAAGA ENSP00000322219.6:n.1905+1079_1905+1100delinsGGGAAGAAGAAGGGGA...
ENST00000339363.7:c.2520+1079_2520+1100delinsGGGAAGAAGAAGGGGAGGAAGA ENSP00000343671.3:n.2520+1079_2520+1100delinsGGGAAGAAGAAGGGGA...
ENST00000378505.6:c.2984_3005delinsGGGAAGAAGAAGGGGAGGAAGA ENSP00000367766.2:p.Gly995=
ENST00000465127.1:c.172-380127_172-380106delinsTCTTCCTCCCCTTCTTCTTCCC ENSP00000417050.1:n.172-380127_172-380106delinsTCTTCCTCCCCTTC...
ENST00000474584.5:c.*37+4944_*37+4965delinsGGGAAGAAGAAGGGGAGGAAGA ENSP00000418926.1:n.*37+4944_*37+4965delinsGGGAAGAAGAAGGGGAGG...
ENST00000482855.5:c.1905+1079_1905+1100delinsGGGAAGAAGAAGGGGAGGAAGA ENSP00000419276.1:n.1905+1079_1905+1100delinsGGGAAGAAGAAGGGGA...
ENST00000494707.5:c.139+4944_139+4965delinsGGGAAGAAGAAGGGGAGGAAGA
NM_000328.2:c.1905+1079_1905+1100delinsGGGAAGAAGAAGGGGAGGAAGA NP_000319.1:n.1905+1079_1905+1100delinsGGGAAGAAGAAGGGGAGGAAGA...
NM_001034853.1:c.2984_3005delinsGGGAAGAAGAAGGGGAGGAAGA NP_001030025.1:p.Gly995=
XM_005272633.1:c.1572+4944_1572+4965delinsGGGAAGAAGAAGGGGAGGAAGA XP_005272690.1:n.1572+4944_1572+4965delinsGGGAAGAAGAAGGGGAGGA...
XM_011543940.1:c.1902+1079_1902+1100delinsGGGAAGAAGAAGGGGAGGAAGA XP_011542242.1:n.1902+1079_1902+1100delinsGGGAAGAAGAAGGGGAGGA...
XM_005272633.3:c.1572+4944_1572+4965delinsGGGAAGAAGAAGGGGAGGAAGA XP_005272690.1:n.1572+4944_1572+4965delinsGGGAAGAAGAAGGGGAGGA...
XM_011543940.3:c.1902+1079_1902+1100delinsGGGAAGAAGAAGGGGAGGAAGA XP_011542242.1:n.1902+1079_1902+1100delinsGGGAAGAAGAAGGGGAGGA...
XM_017029712.2:c.1569+4944_1569+4965delinsGGGAAGAAGAAGGGGAGGAAGA XP_016885201.1:n.1569+4944_1569+4965delinsGGGAAGAAGAAGGGGAGGA...
NM_001367245.1:c.1902+1079_1902+1100delinsGGGAAGAAGAAGGGGAGGAAGA NP_001354174.1:n.1902+1079_1902+1100delinsGGGAAGAAGAAGGGGAGGA...
NM_001367246.1:c.1719+1079_1719+1100delinsGGGAAGAAGAAGGGGAGGAAGA NP_001354175.1:n.1719+1079_1719+1100delinsGGGAAGAAGAAGGGGAGGA...
NM_001367247.1:c.1572+4944_1572+4965delinsGGGAAGAAGAAGGGGAGGAAGA NP_001354176.1:n.1572+4944_1572+4965delinsGGGAAGAAGAAGGGGAGGA...
NM_001367248.1:c.1602+4944_1602+4965delinsGGGAAGAAGAAGGGGAGGAAGA NP_001354177.1:n.1602+4944_1602+4965delinsGGGAAGAAGAAGGGGAGGA...
NM_001367249.1:c.1569+4944_1569+4965delinsGGGAAGAAGAAGGGGAGGAAGA NP_001354178.1:n.1569+4944_1569+4965delinsGGGAAGAAGAAGGGGAGGA...
NM_001367250.1:c.1569+4944_1569+4965delinsGGGAAGAAGAAGGGGAGGAAGA NP_001354179.1:n.1569+4944_1569+4965delinsGGGAAGAAGAAGGGGAGGA...
NM_001367251.1:c.1386+4944_1386+4965delinsGGGAAGAAGAAGGGGAGGAAGA NP_001354180.1:n.1386+4944_1386+4965delinsGGGAAGAAGAAGGGGAGGA...
NR_159803.1:n.2263+1079_2263+1100delinsGGGAAGAAGAAGGGGAGGAAGA
NR_159804.1:n.1648+4944_1648+4965delinsGGGAAGAAGAAGGGGAGGAAGA
NR_159805.1:n.1714+4944_1714+4965delinsGGGAAGAAGAAGGGGAGGAAGA
NR_159806.1:n.1866+1079_1866+1100delinsGGGAAGAAGAAGGGGAGGAAGA
NR_159807.1:n.1622+4944_1622+4965delinsGGGAAGAAGAAGGGGAGGAAGA
NR_159808.1:n.1826+4944_1826+4965delinsGGGAAGAAGAAGGGGAGGAAGA
NM_000328.3:c.1905+1079_1905+1100delinsGGGAAGAAGAAGGGGAGGAAGA NP_000319.1:n.1905+1079_1905+1100delinsGGGAAGAAGAAGGGGAGGAAGA...
NM_001034853.2:c.2984_3005delinsGGGAAGAAGAAGGGGAGGAAGA MANE Select NP_001030025.1:p.Gly995=