Canonical Allele Identifier: CA10385263

Gene: RPGR

Linked Data

• ClinVar Variation Id: 1491495
• ClinVar RCV Id: RCV001986568 ; RCV002464503
• dbSNP Id: rs771584745
• ExAC: X:38145655 TCTC / T
• gnomAD v3: X-38286402-TCTC-T
• gnomAD v4: X-38286402-TCTC-T
• MyVariant Identifiers: chrX:g.38145656_38145658del (hg19) ; chrX:g.38286403_38286405del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38286405_38286407del , CM000685.2:g.38286405_38286407del	GRCh38
NC_000023.10:g.38145658_38145660del , CM000685.1:g.38145658_38145660del	GRCh37
NC_000023.9:g.38030602_38030604del	NCBI36
NG_009553.1:g.46131_46133del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494707.6:c.953+1460_953+1462del
ENST00000642170.1:n.1826+4554_1826+4556del
ENST00000642395.2:c.1905+689_1905+691del	ENSP00000493468.2:n.1905+689_1905+691del
ENST00000642739.1:c.1572+4554_1572+4556del	ENSP00000493596.1:n.1572+4554_1572+4556del
ENST00000644238.1:c.1386+4554_1386+4556del	ENSP00000496728.1:n.1386+4554_1386+4556del
ENST00000644337.1:c.1719+689_1719+691del	ENSP00000494557.1:n.1719+689_1719+691del
ENST00000645032.1:c.2594_2596del MANE Select	ENSP00000495537.1:p.Gly865del
ENST00000645124.1:c.*101+689_*101+691del	ENSP00000496446.1:n.*101+689_*101+691del
ENST00000646020.1:c.*594+689_*594+691del	ENSP00000494745.1:n.*594+689_*594+691del
ENST00000318842.11:c.1905+689_1905+691del	ENSP00000322219.6:n.1905+689_1905+691del
ENST00000339363.7:c.2520+689_2520+691del	ENSP00000343671.3:n.2520+689_2520+691del
ENST00000378505.6:c.2594_2596del	ENSP00000367766.2:p.Gly865del
ENST00000465127.1:c.172-379716_172-379714del	ENSP00000417050.1:n.172-379716_172-379714del
ENST00000474584.5:c.*37+4554_*37+4556del	ENSP00000418926.1:n.*37+4554_*37+4556del
ENST00000482855.5:c.1905+689_1905+691del	ENSP00000419276.1:n.1905+689_1905+691del
ENST00000494707.5:c.139+4554_139+4556del
NM_000328.2:c.1905+689_1905+691del	NP_000319.1:n.1905+689_1905+691del
NM_001034853.1:c.2594_2596del	NP_001030025.1:p.Gly865del
XM_005272633.1:c.1572+4554_1572+4556del	XP_005272690.1:n.1572+4554_1572+4556del
XM_011543940.1:c.1902+689_1902+691del	XP_011542242.1:n.1902+689_1902+691del
XM_005272633.3:c.1572+4554_1572+4556del	XP_005272690.1:n.1572+4554_1572+4556del
XM_011543940.3:c.1902+689_1902+691del	XP_011542242.1:n.1902+689_1902+691del
XM_017029712.2:c.1569+4554_1569+4556del	XP_016885201.1:n.1569+4554_1569+4556del
NM_001367245.1:c.1902+689_1902+691del	NP_001354174.1:n.1902+689_1902+691del
NM_001367246.1:c.1719+689_1719+691del	NP_001354175.1:n.1719+689_1719+691del
NM_001367247.1:c.1572+4554_1572+4556del	NP_001354176.1:n.1572+4554_1572+4556del
NM_001367248.1:c.1602+4554_1602+4556del	NP_001354177.1:n.1602+4554_1602+4556del
NM_001367249.1:c.1569+4554_1569+4556del	NP_001354178.1:n.1569+4554_1569+4556del
NM_001367250.1:c.1569+4554_1569+4556del	NP_001354179.1:n.1569+4554_1569+4556del
NM_001367251.1:c.1386+4554_1386+4556del	NP_001354180.1:n.1386+4554_1386+4556del
NR_159803.1:n.2263+689_2263+691del
NR_159804.1:n.1648+4554_1648+4556del
NR_159805.1:n.1714+4554_1714+4556del
NR_159806.1:n.1866+689_1866+691del
NR_159807.1:n.1622+4554_1622+4556del
NR_159808.1:n.1826+4554_1826+4556del
NM_000328.3:c.1905+689_1905+691del	NP_000319.1:n.1905+689_1905+691del
NM_001034853.2:c.2594_2596del MANE Select	NP_001030025.1:p.Gly865del