Canonical Allele Identifier: CA2424844687

Gene: RPGR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38286414_38286417delinsCCTT , CM000685.2:g.38286414_38286417delinsCCTT	GRCh38
NC_000023.10:g.38145667_38145670delinsCCTT , CM000685.1:g.38145667_38145670delinsCCTT	GRCh37
NC_000023.9:g.38030611_38030614delinsCCTT	NCBI36
NG_009553.1:g.46119_46122delinsAAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494707.6:c.953+1448_953+1451delinsAAGG
ENST00000642170.1:n.1826+4542_1826+4545delinsAAGG
ENST00000642395.2:c.1905+677_1905+680delinsAAGG	ENSP00000493468.2:n.1905+677_1905+680delinsAAGG
ENST00000642739.1:c.1572+4542_1572+4545delinsAAGG	ENSP00000493596.1:n.1572+4542_1572+4545delinsAAGG
ENST00000644238.1:c.1386+4542_1386+4545delinsAAGG	ENSP00000496728.1:n.1386+4542_1386+4545delinsAAGG
ENST00000644337.1:c.1719+677_1719+680delinsAAGG	ENSP00000494557.1:n.1719+677_1719+680delinsAAGG
ENST00000645032.1:c.2582_2585delinsAAGG MANE Select	ENSP00000495537.1:p.Glu861=
ENST00000645124.1:c.*101+677_*101+680delinsAAGG	ENSP00000496446.1:n.*101+677_*101+680delinsAAGG
ENST00000646020.1:c.*594+677_*594+680delinsAAGG	ENSP00000494745.1:n.*594+677_*594+680delinsAAGG
ENST00000318842.11:c.1905+677_1905+680delinsAAGG	ENSP00000322219.6:n.1905+677_1905+680delinsAAGG
ENST00000339363.7:c.2520+677_2520+680delinsAAGG	ENSP00000343671.3:n.2520+677_2520+680delinsAAGG
ENST00000378505.6:c.2582_2585delinsAAGG	ENSP00000367766.2:p.Glu861=
ENST00000465127.1:c.172-379707_172-379704delinsCCTT	ENSP00000417050.1:n.172-379707_172-379704delinsCCTT
ENST00000474584.5:c.*37+4542_*37+4545delinsAAGG	ENSP00000418926.1:n.*37+4542_*37+4545delinsAAGG
ENST00000482855.5:c.1905+677_1905+680delinsAAGG	ENSP00000419276.1:n.1905+677_1905+680delinsAAGG
ENST00000494707.5:c.139+4542_139+4545delinsAAGG
NM_000328.2:c.1905+677_1905+680delinsAAGG	NP_000319.1:n.1905+677_1905+680delinsAAGG
NM_001034853.1:c.2582_2585delinsAAGG	NP_001030025.1:p.Glu861=
XM_005272633.1:c.1572+4542_1572+4545delinsAAGG	XP_005272690.1:n.1572+4542_1572+4545delinsAAGG
XM_011543940.1:c.1902+677_1902+680delinsAAGG	XP_011542242.1:n.1902+677_1902+680delinsAAGG
XM_005272633.3:c.1572+4542_1572+4545delinsAAGG	XP_005272690.1:n.1572+4542_1572+4545delinsAAGG
XM_011543940.3:c.1902+677_1902+680delinsAAGG	XP_011542242.1:n.1902+677_1902+680delinsAAGG
XM_017029712.2:c.1569+4542_1569+4545delinsAAGG	XP_016885201.1:n.1569+4542_1569+4545delinsAAGG
NM_001367245.1:c.1902+677_1902+680delinsAAGG	NP_001354174.1:n.1902+677_1902+680delinsAAGG
NM_001367246.1:c.1719+677_1719+680delinsAAGG	NP_001354175.1:n.1719+677_1719+680delinsAAGG
NM_001367247.1:c.1572+4542_1572+4545delinsAAGG	NP_001354176.1:n.1572+4542_1572+4545delinsAAGG
NM_001367248.1:c.1602+4542_1602+4545delinsAAGG	NP_001354177.1:n.1602+4542_1602+4545delinsAAGG
NM_001367249.1:c.1569+4542_1569+4545delinsAAGG	NP_001354178.1:n.1569+4542_1569+4545delinsAAGG
NM_001367250.1:c.1569+4542_1569+4545delinsAAGG	NP_001354179.1:n.1569+4542_1569+4545delinsAAGG
NM_001367251.1:c.1386+4542_1386+4545delinsAAGG	NP_001354180.1:n.1386+4542_1386+4545delinsAAGG
NR_159803.1:n.2263+677_2263+680delinsAAGG
NR_159804.1:n.1648+4542_1648+4545delinsAAGG
NR_159805.1:n.1714+4542_1714+4545delinsAAGG
NR_159806.1:n.1866+677_1866+680delinsAAGG
NR_159807.1:n.1622+4542_1622+4545delinsAAGG
NR_159808.1:n.1826+4542_1826+4545delinsAAGG
NM_000328.3:c.1905+677_1905+680delinsAAGG	NP_000319.1:n.1905+677_1905+680delinsAAGG
NM_001034853.2:c.2582_2585delinsAAGG MANE Select	NP_001030025.1:p.Glu861=