Canonical Allele Identifier: CA1139667408

Gene: RPGR

Linked Data

• ClinVar Variation Id: 975122
• ClinVar RCV Id: RCV001251538
• dbSNP Id: rs2067135227

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38286038_38286057del , CM000685.2:g.38286038_38286057del	GRCh38
NC_000023.10:g.38145291_38145310del , CM000685.1:g.38145291_38145310del	GRCh37
NC_000023.9:g.38030235_38030254del	NCBI36
NG_009553.1:g.46482_46501del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494707.6:c.953+1811_953+1830del
ENST00000642170.1:n.1826+4905_1826+4924del
ENST00000642395.2:c.1905+1040_1905+1059del	ENSP00000493468.2:n.1905+1040_1905+1059del
ENST00000642739.1:c.1572+4905_1572+4924del	ENSP00000493596.1:n.1572+4905_1572+4924del
ENST00000644238.1:c.1386+4905_1386+4924del	ENSP00000496728.1:n.1386+4905_1386+4924del
ENST00000644337.1:c.1719+1040_1719+1059del	ENSP00000494557.1:n.1719+1040_1719+1059del
ENST00000645032.1:c.2945_2964del MANE Select	ENSP00000495537.1:p.Glu982GlyfsTer?
ENST00000645124.1:c.*101+1040_*101+1059del	ENSP00000496446.1:n.*101+1040_*101+1059del
ENST00000646020.1:c.*594+1040_*594+1059del	ENSP00000494745.1:n.*594+1040_*594+1059del
ENST00000318842.11:c.1905+1040_1905+1059del	ENSP00000322219.6:n.1905+1040_1905+1059del
ENST00000339363.7:c.2520+1040_2520+1059del	ENSP00000343671.3:n.2520+1040_2520+1059del
ENST00000378505.6:c.2945_2964del	ENSP00000367766.2:p.Glu982GlyfsTer?
ENST00000465127.1:c.172-380083_172-380064del	ENSP00000417050.1:n.172-380083_172-380064del
ENST00000474584.5:c.*37+4905_*37+4924del	ENSP00000418926.1:n.*37+4905_*37+4924del
ENST00000482855.5:c.1905+1040_1905+1059del	ENSP00000419276.1:n.1905+1040_1905+1059del
ENST00000494707.5:c.139+4905_139+4924del
NM_000328.2:c.1905+1040_1905+1059del	NP_000319.1:n.1905+1040_1905+1059del
NM_001034853.1:c.2945_2964del	NP_001030025.1:p.Glu982GlyfsTer?
XM_005272633.1:c.1572+4905_1572+4924del	XP_005272690.1:n.1572+4905_1572+4924del
XM_011543940.1:c.1902+1040_1902+1059del	XP_011542242.1:n.1902+1040_1902+1059del
XM_005272633.3:c.1572+4905_1572+4924del	XP_005272690.1:n.1572+4905_1572+4924del
XM_011543940.3:c.1902+1040_1902+1059del	XP_011542242.1:n.1902+1040_1902+1059del
XM_017029712.2:c.1569+4905_1569+4924del	XP_016885201.1:n.1569+4905_1569+4924del
NM_001367245.1:c.1902+1040_1902+1059del	NP_001354174.1:n.1902+1040_1902+1059del
NM_001367246.1:c.1719+1040_1719+1059del	NP_001354175.1:n.1719+1040_1719+1059del
NM_001367247.1:c.1572+4905_1572+4924del	NP_001354176.1:n.1572+4905_1572+4924del
NM_001367248.1:c.1602+4905_1602+4924del	NP_001354177.1:n.1602+4905_1602+4924del
NM_001367249.1:c.1569+4905_1569+4924del	NP_001354178.1:n.1569+4905_1569+4924del
NM_001367250.1:c.1569+4905_1569+4924del	NP_001354179.1:n.1569+4905_1569+4924del
NM_001367251.1:c.1386+4905_1386+4924del	NP_001354180.1:n.1386+4905_1386+4924del
NR_159803.1:n.2263+1040_2263+1059del
NR_159804.1:n.1648+4905_1648+4924del
NR_159805.1:n.1714+4905_1714+4924del
NR_159806.1:n.1866+1040_1866+1059del
NR_159807.1:n.1622+4905_1622+4924del
NR_159808.1:n.1826+4905_1826+4924del
NM_000328.3:c.1905+1040_1905+1059del	NP_000319.1:n.1905+1040_1905+1059del
NM_001034853.2:c.2945_2964del MANE Select	NP_001030025.1:p.Glu982GlyfsTer?