Canonical Allele Identifier: CA2697553045

Gene: RPGR

Linked Data

• ClinVar Variation Id: 2747881
• ClinVar RCV Id: RCV003536611

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38286034_38286179del , CM000685.2:g.38286034_38286179del	GRCh38
NC_000023.10:g.38145287_38145432del , CM000685.1:g.38145287_38145432del	GRCh37
NC_000023.9:g.38030231_38030376del	NCBI36
NG_009553.1:g.46362_46507del

Transcript Alleles

HGVS	Amino-acid change
ENST00000494707.6:c.953+1691_953+1836del
ENST00000642170.1:n.1826+4785_1826+4930del
ENST00000642395.2:c.1905+920_1905+1065del	ENSP00000493468.2:n.1905+920_1905+1065del...
ENST00000642739.1:c.1572+4785_1572+4930del	ENSP00000493596.1:n.1572+4785_1572+4930de...
ENST00000644238.1:c.1386+4785_1386+4930del	ENSP00000496728.1:n.1386+4785_1386+4930de...
ENST00000644337.1:c.1719+920_1719+1065del	ENSP00000494557.1:n.1719+920_1719+1065del...
ENST00000645032.1:c.2825_2970del MANE Select	ENSP00000495537.1:p.Glu942GlyfsTer?
ENST00000645124.1:c.*101+920_*101+1065del	ENSP00000496446.1:n.*101+920_*101+1065del...
ENST00000646020.1:c.*594+920_*594+1065del	ENSP00000494745.1:n.*594+920_*594+1065del...
ENST00000318842.11:c.1905+920_1905+1065del	ENSP00000322219.6:n.1905+920_1905+1065del...
ENST00000339363.7:c.2520+920_2520+1065del	ENSP00000343671.3:n.2520+920_2520+1065del...
ENST00000378505.6:c.2825_2970del	ENSP00000367766.2:p.Glu942GlyfsTer?
ENST00000465127.1:c.172-380087_172-379942del	ENSP00000417050.1:n.172-380087_172-379942...
ENST00000474584.5:c.*37+4785_*37+4930del	ENSP00000418926.1:n.*37+4785_*37+4930del
ENST00000482855.5:c.1905+920_1905+1065del	ENSP00000419276.1:n.1905+920_1905+1065del...
ENST00000494707.5:c.139+4785_139+4930del
NM_000328.2:c.1905+920_1905+1065del	NP_000319.1:n.1905+920_1905+1065del
NM_001034853.1:c.2825_2970del	NP_001030025.1:p.Glu942GlyfsTer?
XM_005272633.1:c.1572+4785_1572+4930del	XP_005272690.1:n.1572+4785_1572+4930del
XM_011543940.1:c.1902+920_1902+1065del	XP_011542242.1:n.1902+920_1902+1065del
XM_005272633.3:c.1572+4785_1572+4930del	XP_005272690.1:n.1572+4785_1572+4930del
XM_011543940.3:c.1902+920_1902+1065del	XP_011542242.1:n.1902+920_1902+1065del
XM_017029712.2:c.1569+4785_1569+4930del	XP_016885201.1:n.1569+4785_1569+4930del
NM_001367245.1:c.1902+920_1902+1065del	NP_001354174.1:n.1902+920_1902+1065del
NM_001367246.1:c.1719+920_1719+1065del	NP_001354175.1:n.1719+920_1719+1065del
NM_001367247.1:c.1572+4785_1572+4930del	NP_001354176.1:n.1572+4785_1572+4930del
NM_001367248.1:c.1602+4785_1602+4930del	NP_001354177.1:n.1602+4785_1602+4930del
NM_001367249.1:c.1569+4785_1569+4930del	NP_001354178.1:n.1569+4785_1569+4930del
NM_001367250.1:c.1569+4785_1569+4930del	NP_001354179.1:n.1569+4785_1569+4930del
NM_001367251.1:c.1386+4785_1386+4930del	NP_001354180.1:n.1386+4785_1386+4930del
NR_159803.1:n.2263+920_2263+1065del
NR_159804.1:n.1648+4785_1648+4930del
NR_159805.1:n.1714+4785_1714+4930del
NR_159806.1:n.1866+920_1866+1065del
NR_159807.1:n.1622+4785_1622+4930del
NR_159808.1:n.1826+4785_1826+4930del
NM_000328.3:c.1905+920_1905+1065del	NP_000319.1:n.1905+920_1905+1065del
NM_001034853.2:c.2825_2970del MANE Select	NP_001030025.1:p.Glu942GlyfsTer?