Canonical Allele Identifier: CA2579984164

Gene: RPGR

Linked Data

• ClinVar Variation Id: 2500933
• ClinVar RCV Id: RCV003226118

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38286526_38286596dup , CM000685.2:g.38286526_38286596dup	GRCh38
NC_000023.10:g.38145779_38145849dup , CM000685.1:g.38145779_38145849dup	GRCh37
NC_000023.9:g.38030723_38030793dup	NCBI36
NG_009553.1:g.45946_46016dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000494707.6:c.953+1275_953+1345dup
ENST00000642170.1:n.1826+4369_1826+4439dup
ENST00000642395.2:c.1905+504_1905+574dup	ENSP00000493468.2:n.1905+504_1905+574dup
ENST00000642739.1:c.1572+4369_1572+4439dup	ENSP00000493596.1:n.1572+4369_1572+4439du...
ENST00000644238.1:c.1386+4369_1386+4439dup	ENSP00000496728.1:n.1386+4369_1386+4439du...
ENST00000644337.1:c.1719+504_1719+574dup	ENSP00000494557.1:n.1719+504_1719+574dup
ENST00000645032.1:c.2409_2479dup MANE Select	ENSP00000495537.1:p.Glu827GlyfsTer12
ENST00000645124.1:c.*101+504_*101+574dup	ENSP00000496446.1:n.*101+504_*101+574dup
ENST00000646020.1:c.*594+504_*594+574dup	ENSP00000494745.1:n.*594+504_*594+574dup
ENST00000318842.11:c.1905+504_1905+574dup	ENSP00000322219.6:n.1905+504_1905+574dup
ENST00000339363.7:c.2520+504_2520+574dup	ENSP00000343671.3:n.2520+504_2520+574dup
ENST00000378505.6:c.2409_2479dup	ENSP00000367766.2:p.Glu827GlyfsTer12
ENST00000465127.1:c.172-379595_172-379525dup	ENSP00000417050.1:n.172-379595_172-379525...
ENST00000474584.5:c.*37+4369_*37+4439dup	ENSP00000418926.1:n.*37+4369_*37+4439dup
ENST00000482855.5:c.1905+504_1905+574dup	ENSP00000419276.1:n.1905+504_1905+574dup
ENST00000494707.5:c.139+4369_139+4439dup
NM_000328.2:c.1905+504_1905+574dup	NP_000319.1:n.1905+504_1905+574dup
NM_001034853.1:c.2409_2479dup	NP_001030025.1:p.Glu827GlyfsTer12
XM_005272633.1:c.1572+4369_1572+4439dup	XP_005272690.1:n.1572+4369_1572+4439dup
XM_011543940.1:c.1902+504_1902+574dup	XP_011542242.1:n.1902+504_1902+574dup
XM_005272633.3:c.1572+4369_1572+4439dup	XP_005272690.1:n.1572+4369_1572+4439dup
XM_011543940.3:c.1902+504_1902+574dup	XP_011542242.1:n.1902+504_1902+574dup
XM_017029712.2:c.1569+4369_1569+4439dup	XP_016885201.1:n.1569+4369_1569+4439dup
NM_001367245.1:c.1902+504_1902+574dup	NP_001354174.1:n.1902+504_1902+574dup
NM_001367246.1:c.1719+504_1719+574dup	NP_001354175.1:n.1719+504_1719+574dup
NM_001367247.1:c.1572+4369_1572+4439dup	NP_001354176.1:n.1572+4369_1572+4439dup
NM_001367248.1:c.1602+4369_1602+4439dup	NP_001354177.1:n.1602+4369_1602+4439dup
NM_001367249.1:c.1569+4369_1569+4439dup	NP_001354178.1:n.1569+4369_1569+4439dup
NM_001367250.1:c.1569+4369_1569+4439dup	NP_001354179.1:n.1569+4369_1569+4439dup
NM_001367251.1:c.1386+4369_1386+4439dup	NP_001354180.1:n.1386+4369_1386+4439dup
NR_159803.1:n.2263+504_2263+574dup
NR_159804.1:n.1648+4369_1648+4439dup
NR_159805.1:n.1714+4369_1714+4439dup
NR_159806.1:n.1866+504_1866+574dup
NR_159807.1:n.1622+4369_1622+4439dup
NR_159808.1:n.1826+4369_1826+4439dup
NM_000328.3:c.1905+504_1905+574dup	NP_000319.1:n.1905+504_1905+574dup
NM_001034853.2:c.2409_2479dup MANE Select	NP_001030025.1:p.Glu827GlyfsTer12