Canonical Allele Identifier: CA2424844271

Gene: RPGR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38285970_38285973delinsTCCC , CM000685.2:g.38285970_38285973delinsTCCC	GRCh38
NC_000023.10:g.38145223_38145226delinsTCCC , CM000685.1:g.38145223_38145226delinsTCCC	GRCh37
NC_000023.9:g.38030167_38030170delinsTCCC	NCBI36
NG_009553.1:g.46563_46566delinsGGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494707.6:c.953+1892_953+1895delinsGGGA
ENST00000642170.1:n.1826+4986_1826+4989delinsGGGA
ENST00000642395.2:c.1905+1121_1905+1124delinsGGGA	ENSP00000493468.2:n.1905+1121_1905+1124delinsGGGA
ENST00000642739.1:c.1572+4986_1572+4989delinsGGGA	ENSP00000493596.1:n.1572+4986_1572+4989delinsGGGA
ENST00000644238.1:c.1386+4986_1386+4989delinsGGGA	ENSP00000496728.1:n.1386+4986_1386+4989delinsGGGA
ENST00000644337.1:c.1719+1121_1719+1124delinsGGGA	ENSP00000494557.1:n.1719+1121_1719+1124delinsGGGA
ENST00000645032.1:c.3026_3029delinsGGGA MANE Select	ENSP00000495537.1:p.Gly1009=
ENST00000645124.1:c.*101+1121_*101+1124delinsGGGA	ENSP00000496446.1:n.*101+1121_*101+1124delinsGGGA
ENST00000646020.1:c.*594+1121_*594+1124delinsGGGA	ENSP00000494745.1:n.*594+1121_*594+1124delinsGGGA
ENST00000318842.11:c.1905+1121_1905+1124delinsGGGA	ENSP00000322219.6:n.1905+1121_1905+1124delinsGGGA
ENST00000339363.7:c.2520+1121_2520+1124delinsGGGA	ENSP00000343671.3:n.2520+1121_2520+1124delinsGGGA
ENST00000378505.6:c.3026_3029delinsGGGA	ENSP00000367766.2:p.Gly1009=
ENST00000465127.1:c.172-380151_172-380148delinsTCCC	ENSP00000417050.1:n.172-380151_172-380148delinsTCCC
ENST00000474584.5:c.*37+4986_*37+4989delinsGGGA	ENSP00000418926.1:n.*37+4986_*37+4989delinsGGGA
ENST00000482855.5:c.1905+1121_1905+1124delinsGGGA	ENSP00000419276.1:n.1905+1121_1905+1124delinsGGGA
ENST00000494707.5:c.139+4986_139+4989delinsGGGA
NM_000328.2:c.1905+1121_1905+1124delinsGGGA	NP_000319.1:n.1905+1121_1905+1124delinsGGGA
NM_001034853.1:c.3026_3029delinsGGGA	NP_001030025.1:p.Gly1009=
XM_005272633.1:c.1572+4986_1572+4989delinsGGGA	XP_005272690.1:n.1572+4986_1572+4989delinsGGGA
XM_011543940.1:c.1902+1121_1902+1124delinsGGGA	XP_011542242.1:n.1902+1121_1902+1124delinsGGGA
XM_005272633.3:c.1572+4986_1572+4989delinsGGGA	XP_005272690.1:n.1572+4986_1572+4989delinsGGGA
XM_011543940.3:c.1902+1121_1902+1124delinsGGGA	XP_011542242.1:n.1902+1121_1902+1124delinsGGGA
XM_017029712.2:c.1569+4986_1569+4989delinsGGGA	XP_016885201.1:n.1569+4986_1569+4989delinsGGGA
NM_001367245.1:c.1902+1121_1902+1124delinsGGGA	NP_001354174.1:n.1902+1121_1902+1124delinsGGGA
NM_001367246.1:c.1719+1121_1719+1124delinsGGGA	NP_001354175.1:n.1719+1121_1719+1124delinsGGGA
NM_001367247.1:c.1572+4986_1572+4989delinsGGGA	NP_001354176.1:n.1572+4986_1572+4989delinsGGGA
NM_001367248.1:c.1602+4986_1602+4989delinsGGGA	NP_001354177.1:n.1602+4986_1602+4989delinsGGGA
NM_001367249.1:c.1569+4986_1569+4989delinsGGGA	NP_001354178.1:n.1569+4986_1569+4989delinsGGGA
NM_001367250.1:c.1569+4986_1569+4989delinsGGGA	NP_001354179.1:n.1569+4986_1569+4989delinsGGGA
NM_001367251.1:c.1386+4986_1386+4989delinsGGGA	NP_001354180.1:n.1386+4986_1386+4989delinsGGGA
NR_159803.1:n.2263+1121_2263+1124delinsGGGA
NR_159804.1:n.1648+4986_1648+4989delinsGGGA
NR_159805.1:n.1714+4986_1714+4989delinsGGGA
NR_159806.1:n.1866+1121_1866+1124delinsGGGA
NR_159807.1:n.1622+4986_1622+4989delinsGGGA
NR_159808.1:n.1826+4986_1826+4989delinsGGGA
NM_000328.3:c.1905+1121_1905+1124delinsGGGA	NP_000319.1:n.1905+1121_1905+1124delinsGGGA
NM_001034853.2:c.3026_3029delinsGGGA MANE Select	NP_001030025.1:p.Gly1009=