Canonical Allele Identifier: CA2837967741

Gene: RPGR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38286177_38286197del , CM000685.2:g.38286177_38286197del	GRCh38
NC_000023.10:g.38145430_38145450del , CM000685.1:g.38145430_38145450del	GRCh37
NC_000023.9:g.38030374_38030394del	NCBI36
NG_009553.1:g.46345_46365del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494707.6:c.953+1674_953+1694del
ENST00000642170.1:n.1826+4768_1826+4788del
ENST00000642395.2:c.1905+903_1905+923del	ENSP00000493468.2:n.1905+903_1905+923del
ENST00000642739.1:c.1572+4768_1572+4788del	ENSP00000493596.1:n.1572+4768_1572+4788del
ENST00000644238.1:c.1386+4768_1386+4788del	ENSP00000496728.1:n.1386+4768_1386+4788del
ENST00000644337.1:c.1719+903_1719+923del	ENSP00000494557.1:n.1719+903_1719+923del
ENST00000645032.1:c.2808_2828del MANE Select	ENSP00000495537.1:p.Glu936_Glu942del
ENST00000645124.1:c.*101+903_*101+923del	ENSP00000496446.1:n.*101+903_*101+923del
ENST00000646020.1:c.*594+903_*594+923del	ENSP00000494745.1:n.*594+903_*594+923del
ENST00000318842.11:c.1905+903_1905+923del	ENSP00000322219.6:n.1905+903_1905+923del
ENST00000339363.7:c.2520+903_2520+923del	ENSP00000343671.3:n.2520+903_2520+923del
ENST00000378505.6:c.2808_2828del	ENSP00000367766.2:p.Glu936_Glu942del
ENST00000465127.1:c.172-379944_172-379924del	ENSP00000417050.1:n.172-379944_172-379924del
ENST00000474584.5:c.*37+4768_*37+4788del	ENSP00000418926.1:n.*37+4768_*37+4788del
ENST00000482855.5:c.1905+903_1905+923del	ENSP00000419276.1:n.1905+903_1905+923del
ENST00000494707.5:c.139+4768_139+4788del
NM_000328.2:c.1905+903_1905+923del	NP_000319.1:n.1905+903_1905+923del
NM_001034853.1:c.2808_2828del	NP_001030025.1:p.Glu936_Glu942del
XM_005272633.1:c.1572+4768_1572+4788del	XP_005272690.1:n.1572+4768_1572+4788del
XM_011543940.1:c.1902+903_1902+923del	XP_011542242.1:n.1902+903_1902+923del
XM_005272633.3:c.1572+4768_1572+4788del	XP_005272690.1:n.1572+4768_1572+4788del
XM_011543940.3:c.1902+903_1902+923del	XP_011542242.1:n.1902+903_1902+923del
XM_017029712.2:c.1569+4768_1569+4788del	XP_016885201.1:n.1569+4768_1569+4788del
NM_001367245.1:c.1902+903_1902+923del	NP_001354174.1:n.1902+903_1902+923del
NM_001367246.1:c.1719+903_1719+923del	NP_001354175.1:n.1719+903_1719+923del
NM_001367247.1:c.1572+4768_1572+4788del	NP_001354176.1:n.1572+4768_1572+4788del
NM_001367248.1:c.1602+4768_1602+4788del	NP_001354177.1:n.1602+4768_1602+4788del
NM_001367249.1:c.1569+4768_1569+4788del	NP_001354178.1:n.1569+4768_1569+4788del
NM_001367250.1:c.1569+4768_1569+4788del	NP_001354179.1:n.1569+4768_1569+4788del
NM_001367251.1:c.1386+4768_1386+4788del	NP_001354180.1:n.1386+4768_1386+4788del
NR_159803.1:n.2263+903_2263+923del
NR_159804.1:n.1648+4768_1648+4788del
NR_159805.1:n.1714+4768_1714+4788del
NR_159806.1:n.1866+903_1866+923del
NR_159807.1:n.1622+4768_1622+4788del
NR_159808.1:n.1826+4768_1826+4788del
NM_000328.3:c.1905+903_1905+923del	NP_000319.1:n.1905+903_1905+923del
NM_001034853.2:c.2808_2828del MANE Select	NP_001030025.1:p.Glu936_Glu942del