Canonical Allele Identifier: CA10385292

Gene: RPGR

Linked Data

• ClinVar Variation Id: 446048
• ClinVar RCV Id: RCV000515047 ; RCV002060225
• dbSNP Id: rs201730068
• ExAC: X:38145915 TTCC / T
• gnomAD v2: X-38145915-TTCC-T
• gnomAD v3: X-38286662-TTCC-T
• gnomAD v4: X-38286662-TTCC-T
• MyVariant Identifiers: chrX:g.38145916_38145918del (hg19) ; chrX:g.38286664_38286666del (hg38) ; chrX:g.38286663_38286665del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38286667_38286669del , CM000685.2:g.38286667_38286669del	GRCh38
NC_000023.10:g.38145920_38145922del , CM000685.1:g.38145920_38145922del	GRCh37
NC_000023.9:g.38030864_38030866del	NCBI36
NG_009553.1:g.45871_45873del

Transcript Alleles

HGVS	Amino-acid change
ENST00000494707.6:c.953+1200_953+1202del
ENST00000642170.1:n.1826+4294_1826+4296del
ENST00000642395.2:c.1905+429_1905+431del	ENSP00000493468.2:n.1905+429_1905+431del
ENST00000642739.1:c.1572+4294_1572+4296del	ENSP00000493596.1:n.1572+4294_1572+4296de...
ENST00000644238.1:c.1386+4294_1386+4296del	ENSP00000496728.1:n.1386+4294_1386+4296de...
ENST00000644337.1:c.1719+429_1719+431del	ENSP00000494557.1:n.1719+429_1719+431del
ENST00000645032.1:c.2334_2336del MANE Select	ENSP00000495537.1:p.Glu779del
ENST00000645124.1:c.*101+429_*101+431del	ENSP00000496446.1:n.*101+429_*101+431del
ENST00000646020.1:c.*594+429_*594+431del	ENSP00000494745.1:n.*594+429_*594+431del
ENST00000318842.11:c.1905+429_1905+431del	ENSP00000322219.6:n.1905+429_1905+431del
ENST00000339363.7:c.2520+429_2520+431del	ENSP00000343671.3:n.2520+429_2520+431del
ENST00000378505.6:c.2334_2336del	ENSP00000367766.2:p.Glu779del
ENST00000465127.1:c.172-379454_172-379452del	ENSP00000417050.1:n.172-379454_172-379452...
ENST00000474584.5:c.*37+4294_*37+4296del	ENSP00000418926.1:n.*37+4294_*37+4296del
ENST00000482855.5:c.1905+429_1905+431del	ENSP00000419276.1:n.1905+429_1905+431del
ENST00000494707.5:c.139+4294_139+4296del
NM_000328.2:c.1905+429_1905+431del	NP_000319.1:n.1905+429_1905+431del
NM_001034853.1:c.2334_2336del	NP_001030025.1:p.Glu779del
XM_005272633.1:c.1572+4294_1572+4296del	XP_005272690.1:n.1572+4294_1572+4296del
XM_011543940.1:c.1902+429_1902+431del	XP_011542242.1:n.1902+429_1902+431del
XM_005272633.3:c.1572+4294_1572+4296del	XP_005272690.1:n.1572+4294_1572+4296del
XM_011543940.3:c.1902+429_1902+431del	XP_011542242.1:n.1902+429_1902+431del
XM_017029712.2:c.1569+4294_1569+4296del	XP_016885201.1:n.1569+4294_1569+4296del
NM_001367245.1:c.1902+429_1902+431del	NP_001354174.1:n.1902+429_1902+431del
NM_001367246.1:c.1719+429_1719+431del	NP_001354175.1:n.1719+429_1719+431del
NM_001367247.1:c.1572+4294_1572+4296del	NP_001354176.1:n.1572+4294_1572+4296del
NM_001367248.1:c.1602+4294_1602+4296del	NP_001354177.1:n.1602+4294_1602+4296del
NM_001367249.1:c.1569+4294_1569+4296del	NP_001354178.1:n.1569+4294_1569+4296del
NM_001367250.1:c.1569+4294_1569+4296del	NP_001354179.1:n.1569+4294_1569+4296del
NM_001367251.1:c.1386+4294_1386+4296del	NP_001354180.1:n.1386+4294_1386+4296del
NR_159803.1:n.2263+429_2263+431del
NR_159804.1:n.1648+4294_1648+4296del
NR_159805.1:n.1714+4294_1714+4296del
NR_159806.1:n.1866+429_1866+431del
NR_159807.1:n.1622+4294_1622+4296del
NR_159808.1:n.1826+4294_1826+4296del
NM_000328.3:c.1905+429_1905+431del	NP_000319.1:n.1905+429_1905+431del
NM_001034853.2:c.2334_2336del MANE Select	NP_001030025.1:p.Glu779del