Canonical Allele Identifier: CA2580100796

Gene: RPGR

Linked Data

• ClinVar Variation Id: 1802282
• ClinVar RCV Id: RCV002465095

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38285735_38285738del , CM000685.2:g.38285735_38285738del	GRCh38
NC_000023.10:g.38144988_38144991del , CM000685.1:g.38144988_38144991del	GRCh37
NC_000023.9:g.38029932_38029935del	NCBI36
NG_009553.1:g.46800_46803del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494707.6:c.953+2129_953+2132del
ENST00000642170.1:n.1826+5223_1826+5226del
ENST00000642395.2:c.1905+1358_1905+1361del	ENSP00000493468.2:n.1905+1358_1905+1361del
ENST00000642739.1:c.1572+5223_1572+5226del	ENSP00000493596.1:n.1572+5223_1572+5226del
ENST00000644238.1:c.1386+5223_1386+5226del	ENSP00000496728.1:n.1386+5223_1386+5226del
ENST00000644337.1:c.1719+1358_1719+1361del	ENSP00000494557.1:n.1719+1358_1719+1361del
ENST00000645032.1:c.3263_3266del MANE Select	ENSP00000495537.1:p.Val1088AlafsTer3
ENST00000645124.1:c.*101+1358_*101+1361del	ENSP00000496446.1:n.*101+1358_*101+1361del
ENST00000646020.1:c.*594+1358_*594+1361del	ENSP00000494745.1:n.*594+1358_*594+1361del
ENST00000318842.11:c.1905+1358_1905+1361del	ENSP00000322219.6:n.1905+1358_1905+1361del
ENST00000339363.7:c.2520+1358_2520+1361del	ENSP00000343671.3:n.2520+1358_2520+1361del
ENST00000378505.6:c.3263_3266del	ENSP00000367766.2:p.Val1088AlafsTer3
ENST00000465127.1:c.172-380386_172-380383del	ENSP00000417050.1:n.172-380386_172-380383del
ENST00000474584.5:c.*37+5223_*37+5226del	ENSP00000418926.1:n.*37+5223_*37+5226del
ENST00000482855.5:c.1905+1358_1905+1361del	ENSP00000419276.1:n.1905+1358_1905+1361del
ENST00000494707.5:c.139+5223_139+5226del
NM_000328.2:c.1905+1358_1905+1361del	NP_000319.1:n.1905+1358_1905+1361del
NM_001034853.1:c.3263_3266del	NP_001030025.1:p.Val1088AlafsTer3
XM_005272633.1:c.1572+5223_1572+5226del	XP_005272690.1:n.1572+5223_1572+5226del
XM_011543940.1:c.1902+1358_1902+1361del	XP_011542242.1:n.1902+1358_1902+1361del
XM_005272633.3:c.1572+5223_1572+5226del	XP_005272690.1:n.1572+5223_1572+5226del
XM_011543940.3:c.1902+1358_1902+1361del	XP_011542242.1:n.1902+1358_1902+1361del
XM_017029712.2:c.1569+5223_1569+5226del	XP_016885201.1:n.1569+5223_1569+5226del
NM_001367245.1:c.1902+1358_1902+1361del	NP_001354174.1:n.1902+1358_1902+1361del
NM_001367246.1:c.1719+1358_1719+1361del	NP_001354175.1:n.1719+1358_1719+1361del
NM_001367247.1:c.1572+5223_1572+5226del	NP_001354176.1:n.1572+5223_1572+5226del
NM_001367248.1:c.1602+5223_1602+5226del	NP_001354177.1:n.1602+5223_1602+5226del
NM_001367249.1:c.1569+5223_1569+5226del	NP_001354178.1:n.1569+5223_1569+5226del
NM_001367250.1:c.1569+5223_1569+5226del	NP_001354179.1:n.1569+5223_1569+5226del
NM_001367251.1:c.1386+5223_1386+5226del	NP_001354180.1:n.1386+5223_1386+5226del
NR_159803.1:n.2263+1358_2263+1361del
NR_159804.1:n.1648+5223_1648+5226del
NR_159805.1:n.1714+5223_1714+5226del
NR_159806.1:n.1866+1358_1866+1361del
NR_159807.1:n.1622+5223_1622+5226del
NR_159808.1:n.1826+5223_1826+5226del
NM_000328.3:c.1905+1358_1905+1361del	NP_000319.1:n.1905+1358_1905+1361del
NM_001034853.2:c.3263_3266del MANE Select	NP_001030025.1:p.Val1088AlafsTer3