Canonical Allele Identifier: CA2424844515
Gene: RPGR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38286218_38286221delinsTTCC , CM000685.2:g.38286218_38286221delinsTTCC GRCh38
NC_000023.10:g.38145471_38145474delinsTTCC , CM000685.1:g.38145471_38145474delinsTTCC GRCh37
NC_000023.9:g.38030415_38030418delinsTTCC NCBI36
NG_009553.1:g.46315_46318delinsGGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000494707.6:c.953+1644_953+1647delinsGGAA
ENST00000642170.1:n.1826+4738_1826+4741delinsGGAA
ENST00000642395.2:c.1905+873_1905+876delinsGGAA ENSP00000493468.2:n.1905+873_1905+876delinsGGAA
ENST00000642739.1:c.1572+4738_1572+4741delinsGGAA ENSP00000493596.1:n.1572+4738_1572+4741delinsGGAA
ENST00000644238.1:c.1386+4738_1386+4741delinsGGAA ENSP00000496728.1:n.1386+4738_1386+4741delinsGGAA
ENST00000644337.1:c.1719+873_1719+876delinsGGAA ENSP00000494557.1:n.1719+873_1719+876delinsGGAA
ENST00000645032.1:c.2778_2781delinsGGAA MANE Select ENSP00000495537.1:p.Glu926=
ENST00000645124.1:c.*101+873_*101+876delinsGGAA ENSP00000496446.1:n.*101+873_*101+876delinsGGAA
ENST00000646020.1:c.*594+873_*594+876delinsGGAA ENSP00000494745.1:n.*594+873_*594+876delinsGGAA
ENST00000318842.11:c.1905+873_1905+876delinsGGAA ENSP00000322219.6:n.1905+873_1905+876delinsGGAA
ENST00000339363.7:c.2520+873_2520+876delinsGGAA ENSP00000343671.3:n.2520+873_2520+876delinsGGAA
ENST00000378505.6:c.2778_2781delinsGGAA ENSP00000367766.2:p.Glu926=
ENST00000465127.1:c.172-379903_172-379900delinsTTCC ENSP00000417050.1:n.172-379903_172-379900delinsTTCC
ENST00000474584.5:c.*37+4738_*37+4741delinsGGAA ENSP00000418926.1:n.*37+4738_*37+4741delinsGGAA
ENST00000482855.5:c.1905+873_1905+876delinsGGAA ENSP00000419276.1:n.1905+873_1905+876delinsGGAA
ENST00000494707.5:c.139+4738_139+4741delinsGGAA
NM_000328.2:c.1905+873_1905+876delinsGGAA NP_000319.1:n.1905+873_1905+876delinsGGAA
NM_001034853.1:c.2778_2781delinsGGAA NP_001030025.1:p.Glu926=
XM_005272633.1:c.1572+4738_1572+4741delinsGGAA XP_005272690.1:n.1572+4738_1572+4741delinsGGAA
XM_011543940.1:c.1902+873_1902+876delinsGGAA XP_011542242.1:n.1902+873_1902+876delinsGGAA
XM_005272633.3:c.1572+4738_1572+4741delinsGGAA XP_005272690.1:n.1572+4738_1572+4741delinsGGAA
XM_011543940.3:c.1902+873_1902+876delinsGGAA XP_011542242.1:n.1902+873_1902+876delinsGGAA
XM_017029712.2:c.1569+4738_1569+4741delinsGGAA XP_016885201.1:n.1569+4738_1569+4741delinsGGAA
NM_001367245.1:c.1902+873_1902+876delinsGGAA NP_001354174.1:n.1902+873_1902+876delinsGGAA
NM_001367246.1:c.1719+873_1719+876delinsGGAA NP_001354175.1:n.1719+873_1719+876delinsGGAA
NM_001367247.1:c.1572+4738_1572+4741delinsGGAA NP_001354176.1:n.1572+4738_1572+4741delinsGGAA
NM_001367248.1:c.1602+4738_1602+4741delinsGGAA NP_001354177.1:n.1602+4738_1602+4741delinsGGAA
NM_001367249.1:c.1569+4738_1569+4741delinsGGAA NP_001354178.1:n.1569+4738_1569+4741delinsGGAA
NM_001367250.1:c.1569+4738_1569+4741delinsGGAA NP_001354179.1:n.1569+4738_1569+4741delinsGGAA
NM_001367251.1:c.1386+4738_1386+4741delinsGGAA NP_001354180.1:n.1386+4738_1386+4741delinsGGAA
NR_159803.1:n.2263+873_2263+876delinsGGAA
NR_159804.1:n.1648+4738_1648+4741delinsGGAA
NR_159805.1:n.1714+4738_1714+4741delinsGGAA
NR_159806.1:n.1866+873_1866+876delinsGGAA
NR_159807.1:n.1622+4738_1622+4741delinsGGAA
NR_159808.1:n.1826+4738_1826+4741delinsGGAA
NM_000328.3:c.1905+873_1905+876delinsGGAA NP_000319.1:n.1905+873_1905+876delinsGGAA
NM_001034853.2:c.2778_2781delinsGGAA MANE Select NP_001030025.1:p.Glu926=