Canonical Allele Identifier: CA1139667409

Gene: RPGR

Linked Data

• ClinVar Variation Id: 975121
• ClinVar RCV Id: RCV001251537
• dbSNP Id: rs2067136009

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38286041_38286062dup , CM000685.2:g.38286041_38286062dup	GRCh38
NC_000023.10:g.38145294_38145315dup , CM000685.1:g.38145294_38145315dup	GRCh37
NC_000023.9:g.38030238_38030259dup	NCBI36
NG_009553.1:g.46475_46496dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494707.6:c.953+1804_953+1825dup
ENST00000642170.1:n.1826+4898_1826+4919dup
ENST00000642395.2:c.1905+1033_1905+1054dup	ENSP00000493468.2:n.1905+1033_1905+1054dup
ENST00000642739.1:c.1572+4898_1572+4919dup	ENSP00000493596.1:n.1572+4898_1572+4919dup
ENST00000644238.1:c.1386+4898_1386+4919dup	ENSP00000496728.1:n.1386+4898_1386+4919dup
ENST00000644337.1:c.1719+1033_1719+1054dup	ENSP00000494557.1:n.1719+1033_1719+1054dup
ENST00000645032.1:c.2938_2959dup MANE Select	ENSP00000495537.1:p.Glu987GlyfsTer?
ENST00000645124.1:c.*101+1033_*101+1054dup	ENSP00000496446.1:n.*101+1033_*101+1054dup
ENST00000646020.1:c.*594+1033_*594+1054dup	ENSP00000494745.1:n.*594+1033_*594+1054dup
ENST00000318842.11:c.1905+1033_1905+1054dup	ENSP00000322219.6:n.1905+1033_1905+1054dup
ENST00000339363.7:c.2520+1033_2520+1054dup	ENSP00000343671.3:n.2520+1033_2520+1054dup
ENST00000378505.6:c.2938_2959dup	ENSP00000367766.2:p.Glu987GlyfsTer?
ENST00000465127.1:c.172-380080_172-380059dup	ENSP00000417050.1:n.172-380080_172-380059dup
ENST00000474584.5:c.*37+4898_*37+4919dup	ENSP00000418926.1:n.*37+4898_*37+4919dup
ENST00000482855.5:c.1905+1033_1905+1054dup	ENSP00000419276.1:n.1905+1033_1905+1054dup
ENST00000494707.5:c.139+4898_139+4919dup
NM_000328.2:c.1905+1033_1905+1054dup	NP_000319.1:n.1905+1033_1905+1054dup
NM_001034853.1:c.2938_2959dup	NP_001030025.1:p.Glu987GlyfsTer?
XM_005272633.1:c.1572+4898_1572+4919dup	XP_005272690.1:n.1572+4898_1572+4919dup
XM_011543940.1:c.1902+1033_1902+1054dup	XP_011542242.1:n.1902+1033_1902+1054dup
XM_005272633.3:c.1572+4898_1572+4919dup	XP_005272690.1:n.1572+4898_1572+4919dup
XM_011543940.3:c.1902+1033_1902+1054dup	XP_011542242.1:n.1902+1033_1902+1054dup
XM_017029712.2:c.1569+4898_1569+4919dup	XP_016885201.1:n.1569+4898_1569+4919dup
NM_001367245.1:c.1902+1033_1902+1054dup	NP_001354174.1:n.1902+1033_1902+1054dup
NM_001367246.1:c.1719+1033_1719+1054dup	NP_001354175.1:n.1719+1033_1719+1054dup
NM_001367247.1:c.1572+4898_1572+4919dup	NP_001354176.1:n.1572+4898_1572+4919dup
NM_001367248.1:c.1602+4898_1602+4919dup	NP_001354177.1:n.1602+4898_1602+4919dup
NM_001367249.1:c.1569+4898_1569+4919dup	NP_001354178.1:n.1569+4898_1569+4919dup
NM_001367250.1:c.1569+4898_1569+4919dup	NP_001354179.1:n.1569+4898_1569+4919dup
NM_001367251.1:c.1386+4898_1386+4919dup	NP_001354180.1:n.1386+4898_1386+4919dup
NR_159803.1:n.2263+1033_2263+1054dup
NR_159804.1:n.1648+4898_1648+4919dup
NR_159805.1:n.1714+4898_1714+4919dup
NR_159806.1:n.1866+1033_1866+1054dup
NR_159807.1:n.1622+4898_1622+4919dup
NR_159808.1:n.1826+4898_1826+4919dup
NM_000328.3:c.1905+1033_1905+1054dup	NP_000319.1:n.1905+1033_1905+1054dup
NM_001034853.2:c.2938_2959dup MANE Select	NP_001030025.1:p.Glu987GlyfsTer?