Canonical Allele Identifier: CA2424844652
Gene: RPGR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38286378_38286390delinsCCTTCCTCCCCTT , CM000685.2:g.38286378_38286390delinsCCTTCCTCCCCTT GRCh38
NC_000023.10:g.38145631_38145643delinsCCTTCCTCCCCTT , CM000685.1:g.38145631_38145643delinsCCTTCCTCCCCTT GRCh37
NC_000023.9:g.38030575_38030587delinsCCTTCCTCCCCTT NCBI36
NG_009553.1:g.46146_46158delinsAAGGGGAGGAAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000494707.6:c.953+1475_953+1487delinsAAGGGGAGGAAGG
ENST00000642170.1:n.1826+4569_1826+4581delinsAAGGGGAGGAAGG
ENST00000642395.2:c.1905+704_1905+716delinsAAGGGGAGGAAGG ENSP00000493468.2:n.1905+704_1905+716delinsAAGGGGAGGAAGG
ENST00000642739.1:c.1572+4569_1572+4581delinsAAGGGGAGGAAGG ENSP00000493596.1:n.1572+4569_1572+4581delinsAAGGGGAGGAAGG
ENST00000644238.1:c.1386+4569_1386+4581delinsAAGGGGAGGAAGG ENSP00000496728.1:n.1386+4569_1386+4581delinsAAGGGGAGGAAGG
ENST00000644337.1:c.1719+704_1719+716delinsAAGGGGAGGAAGG ENSP00000494557.1:n.1719+704_1719+716delinsAAGGGGAGGAAGG
ENST00000645032.1:c.2609_2621delinsAAGGGGAGGAAGG MANE Select ENSP00000495537.1:p.Glu870=
ENST00000645124.1:c.*101+704_*101+716delinsAAGGGGAGGAAGG ENSP00000496446.1:n.*101+704_*101+716delinsAAGGGGAGGAAGG
ENST00000646020.1:c.*594+704_*594+716delinsAAGGGGAGGAAGG ENSP00000494745.1:n.*594+704_*594+716delinsAAGGGGAGGAAGG
ENST00000318842.11:c.1905+704_1905+716delinsAAGGGGAGGAAGG ENSP00000322219.6:n.1905+704_1905+716delinsAAGGGGAGGAAGG
ENST00000339363.7:c.2520+704_2520+716delinsAAGGGGAGGAAGG ENSP00000343671.3:n.2520+704_2520+716delinsAAGGGGAGGAAGG
ENST00000378505.6:c.2609_2621delinsAAGGGGAGGAAGG ENSP00000367766.2:p.Glu870=
ENST00000465127.1:c.172-379743_172-379731delinsCCTTCCTCCCCTT ENSP00000417050.1:n.172-379743_172-379731delinsCCTTCCTCCCCTT
ENST00000474584.5:c.*37+4569_*37+4581delinsAAGGGGAGGAAGG ENSP00000418926.1:n.*37+4569_*37+4581delinsAAGGGGAGGAAGG
ENST00000482855.5:c.1905+704_1905+716delinsAAGGGGAGGAAGG ENSP00000419276.1:n.1905+704_1905+716delinsAAGGGGAGGAAGG
ENST00000494707.5:c.139+4569_139+4581delinsAAGGGGAGGAAGG
NM_000328.2:c.1905+704_1905+716delinsAAGGGGAGGAAGG NP_000319.1:n.1905+704_1905+716delinsAAGGGGAGGAAGG
NM_001034853.1:c.2609_2621delinsAAGGGGAGGAAGG NP_001030025.1:p.Glu870=
XM_005272633.1:c.1572+4569_1572+4581delinsAAGGGGAGGAAGG XP_005272690.1:n.1572+4569_1572+4581delinsAAGGGGAGGAAGG
XM_011543940.1:c.1902+704_1902+716delinsAAGGGGAGGAAGG XP_011542242.1:n.1902+704_1902+716delinsAAGGGGAGGAAGG
XM_005272633.3:c.1572+4569_1572+4581delinsAAGGGGAGGAAGG XP_005272690.1:n.1572+4569_1572+4581delinsAAGGGGAGGAAGG
XM_011543940.3:c.1902+704_1902+716delinsAAGGGGAGGAAGG XP_011542242.1:n.1902+704_1902+716delinsAAGGGGAGGAAGG
XM_017029712.2:c.1569+4569_1569+4581delinsAAGGGGAGGAAGG XP_016885201.1:n.1569+4569_1569+4581delinsAAGGGGAGGAAGG
NM_001367245.1:c.1902+704_1902+716delinsAAGGGGAGGAAGG NP_001354174.1:n.1902+704_1902+716delinsAAGGGGAGGAAGG
NM_001367246.1:c.1719+704_1719+716delinsAAGGGGAGGAAGG NP_001354175.1:n.1719+704_1719+716delinsAAGGGGAGGAAGG
NM_001367247.1:c.1572+4569_1572+4581delinsAAGGGGAGGAAGG NP_001354176.1:n.1572+4569_1572+4581delinsAAGGGGAGGAAGG
NM_001367248.1:c.1602+4569_1602+4581delinsAAGGGGAGGAAGG NP_001354177.1:n.1602+4569_1602+4581delinsAAGGGGAGGAAGG
NM_001367249.1:c.1569+4569_1569+4581delinsAAGGGGAGGAAGG NP_001354178.1:n.1569+4569_1569+4581delinsAAGGGGAGGAAGG
NM_001367250.1:c.1569+4569_1569+4581delinsAAGGGGAGGAAGG NP_001354179.1:n.1569+4569_1569+4581delinsAAGGGGAGGAAGG
NM_001367251.1:c.1386+4569_1386+4581delinsAAGGGGAGGAAGG NP_001354180.1:n.1386+4569_1386+4581delinsAAGGGGAGGAAGG
NR_159803.1:n.2263+704_2263+716delinsAAGGGGAGGAAGG
NR_159804.1:n.1648+4569_1648+4581delinsAAGGGGAGGAAGG
NR_159805.1:n.1714+4569_1714+4581delinsAAGGGGAGGAAGG
NR_159806.1:n.1866+704_1866+716delinsAAGGGGAGGAAGG
NR_159807.1:n.1622+4569_1622+4581delinsAAGGGGAGGAAGG
NR_159808.1:n.1826+4569_1826+4581delinsAAGGGGAGGAAGG
NM_000328.3:c.1905+704_1905+716delinsAAGGGGAGGAAGG NP_000319.1:n.1905+704_1905+716delinsAAGGGGAGGAAGG
NM_001034853.2:c.2609_2621delinsAAGGGGAGGAAGG MANE Select NP_001030025.1:p.Glu870=