Canonical Allele Identifier: CA2424848834
Gene: RPGR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38299078T= , CM000685.2:g.38299078T= GRCh38
NC_000023.10:g.38158331T= , CM000685.1:g.38158331T= GRCh37
NC_000023.9:g.38043275T= NCBI36
NG_009553.1:g.33458A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000494707.6:c.327A=
ENST00000642170.1:n.1377A=
ENST00000642395.2:c.1123A= ENSP00000493468.2:p.Ile375=
ENST00000642558.1:c.1030A= ENSP00000496427.1:p.Ile344=
ENST00000642739.1:c.1123A= ENSP00000493596.1:p.Ile375=
ENST00000644238.1:c.1060-1626A= ENSP00000496728.1:n.1060-1626A=
ENST00000644337.1:c.1060-1626A= ENSP00000494557.1:n.1060-1626A=
ENST00000645032.1:c.1123A= MANE Select ENSP00000495537.1:p.Ile375=
ENST00000645124.1:c.1123A= ENSP00000496446.1:p.Ile375=
ENST00000646020.1:c.1183A= ENSP00000494745.1:p.Ile395=
ENST00000318842.11:c.1123A= ENSP00000322219.6:p.Ile375=
ENST00000339363.7:c.1123A= ENSP00000343671.3:p.Ile375=
ENST00000378505.6:c.1123A= ENSP00000367766.2:p.Ile375=
ENST00000464437.1:c.189A=
ENST00000465127.1:c.172-367043T= ENSP00000417050.1:n.172-367043T=
ENST00000474584.5:c.1123A= ENSP00000418926.1:p.Ile375=
ENST00000482855.5:c.1123A= ENSP00000419276.1:p.Ile375=
ENST00000494841.1:n.386A=
NM_000328.2:c.1123A= NP_000319.1:p.Ile375=
NM_001034853.1:c.1123A= NP_001030025.1:p.Ile375=
XM_005272633.1:c.1123A= XP_005272690.1:p.Ile375=
XM_011543940.1:c.1120A= XP_011542242.1:p.Ile374=
XM_005272633.3:c.1123A= XP_005272690.1:p.Ile375=
XM_011543940.3:c.1120A= XP_011542242.1:p.Ile374=
XM_017029712.2:c.1120A= XP_016885201.1:p.Ile374=
NM_001367245.1:c.1120A= NP_001354174.1:p.Ile374=
NM_001367246.1:c.1060-1626A= NP_001354175.1:n.1060-1626A=
NM_001367247.1:c.1123A= NP_001354176.1:p.Ile375=
NM_001367248.1:c.1153A= NP_001354177.1:p.Ile385=
NM_001367249.1:c.1120A= NP_001354178.1:p.Ile374=
NM_001367250.1:c.1120A= NP_001354179.1:p.Ile374=
NM_001367251.1:c.1060-1626A= NP_001354180.1:n.1060-1626A=
NR_159803.1:n.1325A=
NR_159804.1:n.1174A=
NR_159805.1:n.1265A=
NR_159806.1:n.1265A=
NR_159807.1:n.1265A=
NR_159808.1:n.1377A=
NM_000328.3:c.1123A= NP_000319.1:p.Ile375=
NM_001034853.2:c.1123A= MANE Select NP_001030025.1:p.Ile375=