Canonical Allele Identifier: CA645616660
Community Standard Title: NM_001034853.2(RPGR):c.2669_2671del (p.Glu890del)
Gene: RPGR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38286329_38286331del , CM000685.2:g.38286329_38286331del GRCh38
NC_000023.10:g.38145582_38145584del , CM000685.1:g.38145582_38145584del GRCh37
NC_000023.9:g.38030526_38030528del NCBI36
NG_009553.1:g.46206_46208del

Transcript Alleles

HGVS Amino-acid Change
NM_001034853.2:c.2669_2671del MANE Select NP_001030025.1:p.Glu890del
ENST00000645032.1:c.2669_2671del MANE Select ENSP00000495537.1:p.Glu890del
NM_000328.2:c.1905+764_1905+766del NP_000319.1:n.1905+764_1905+766del
NM_000328.3:c.1905+764_1905+766del NP_000319.1:n.1905+764_1905+766del
NM_001034853.1:c.2669_2671del NP_001030025.1:p.Glu890del
NM_001367245.1:c.1902+764_1902+766del NP_001354174.1:n.1902+764_1902+766del
NM_001367246.1:c.1719+764_1719+766del NP_001354175.1:n.1719+764_1719+766del
NM_001367247.1:c.1572+4629_1572+4631del NP_001354176.1:n.1572+4629_1572+4631del
NM_001367248.1:c.1602+4629_1602+4631del NP_001354177.1:n.1602+4629_1602+4631del
NM_001367249.1:c.1569+4629_1569+4631del NP_001354178.1:n.1569+4629_1569+4631del
NM_001367250.1:c.1569+4629_1569+4631del NP_001354179.1:n.1569+4629_1569+4631del
NM_001367251.1:c.1386+4629_1386+4631del NP_001354180.1:n.1386+4629_1386+4631del
NR_159803.1:n.2263+764_2263+766del
NR_159804.1:n.1648+4629_1648+4631del
NR_159805.1:n.1714+4629_1714+4631del
NR_159806.1:n.1866+764_1866+766del
NR_159807.1:n.1622+4629_1622+4631del
NR_159808.1:n.1826+4629_1826+4631del
ENST00000318842.11:c.1905+764_1905+766del ENSP00000322219.6:n.1905+764_1905+766del
ENST00000339363.7:c.2520+764_2520+766del ENSP00000343671.3:n.2520+764_2520+766del
ENST00000378505.6:c.2669_2671del ENSP00000367766.2:p.Glu890del
ENST00000465127.1:c.172-379792_172-379790del ENSP00000417050.1:n.172-379792_172-379790del
ENST00000474584.5:c.*37+4629_*37+4631del ENSP00000418926.1:n.*37+4629_*37+4631del
ENST00000482855.5:c.1905+764_1905+766del ENSP00000419276.1:n.1905+764_1905+766del
ENST00000494707.5:c.139+4629_139+4631del
ENST00000494707.6:c.953+1535_953+1537del
ENST00000642170.1:n.1826+4629_1826+4631del
ENST00000642395.2:c.1905+764_1905+766del ENSP00000493468.2:n.1905+764_1905+766del
ENST00000642739.1:c.1572+4629_1572+4631del ENSP00000493596.1:n.1572+4629_1572+4631del
ENST00000644238.1:c.1386+4629_1386+4631del ENSP00000496728.1:n.1386+4629_1386+4631del
ENST00000644337.1:c.1719+764_1719+766del ENSP00000494557.1:n.1719+764_1719+766del
ENST00000645124.1:c.*101+764_*101+766del ENSP00000496446.1:n.*101+764_*101+766del
ENST00000646020.1:c.*594+764_*594+766del ENSP00000494745.1:n.*594+764_*594+766del
XM_005272633.1:c.1572+4629_1572+4631del XP_005272690.1:n.1572+4629_1572+4631del
XM_005272633.3:c.1572+4629_1572+4631del XP_005272690.1:n.1572+4629_1572+4631del
XM_011543940.1:c.1902+764_1902+766del XP_011542242.1:n.1902+764_1902+766del
XM_011543940.3:c.1902+764_1902+766del XP_011542242.1:n.1902+764_1902+766del
XM_017029712.2:c.1569+4629_1569+4631del XP_016885201.1:n.1569+4629_1569+4631del