Canonical Allele Identifier: CA2424844661

Gene: RPGR

Linked Data

• dbSNP Id: rs2067168590

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38286392_38286394del , CM000685.2:g.38286392_38286394del	GRCh38
NC_000023.10:g.38145645_38145647del , CM000685.1:g.38145645_38145647del	GRCh37
NC_000023.9:g.38030589_38030591del	NCBI36
NG_009553.1:g.46146_46148del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494707.6:c.953+1475_953+1477del
ENST00000642170.1:n.1826+4569_1826+4571del
ENST00000642395.2:c.1905+704_1905+706del	ENSP00000493468.2:n.1905+704_1905+706del
ENST00000642739.1:c.1572+4569_1572+4571del	ENSP00000493596.1:n.1572+4569_1572+4571del
ENST00000644238.1:c.1386+4569_1386+4571del	ENSP00000496728.1:n.1386+4569_1386+4571del
ENST00000644337.1:c.1719+704_1719+706del	ENSP00000494557.1:n.1719+704_1719+706del
ENST00000645032.1:c.2609_2611del MANE Select	ENSP00000495537.1:p.Glu870del
ENST00000645124.1:c.*101+704_*101+706del	ENSP00000496446.1:n.*101+704_*101+706del
ENST00000646020.1:c.*594+704_*594+706del	ENSP00000494745.1:n.*594+704_*594+706del
ENST00000318842.11:c.1905+704_1905+706del	ENSP00000322219.6:n.1905+704_1905+706del
ENST00000339363.7:c.2520+704_2520+706del	ENSP00000343671.3:n.2520+704_2520+706del
ENST00000378505.6:c.2609_2611del	ENSP00000367766.2:p.Glu870del
ENST00000465127.1:c.172-379729_172-379727del	ENSP00000417050.1:n.172-379729_172-379727del
ENST00000474584.5:c.*37+4569_*37+4571del	ENSP00000418926.1:n.*37+4569_*37+4571del
ENST00000482855.5:c.1905+704_1905+706del	ENSP00000419276.1:n.1905+704_1905+706del
ENST00000494707.5:c.139+4569_139+4571del
NM_000328.2:c.1905+704_1905+706del	NP_000319.1:n.1905+704_1905+706del
NM_001034853.1:c.2609_2611del	NP_001030025.1:p.Glu870del
XM_005272633.1:c.1572+4569_1572+4571del	XP_005272690.1:n.1572+4569_1572+4571del
XM_011543940.1:c.1902+704_1902+706del	XP_011542242.1:n.1902+704_1902+706del
XM_005272633.3:c.1572+4569_1572+4571del	XP_005272690.1:n.1572+4569_1572+4571del
XM_011543940.3:c.1902+704_1902+706del	XP_011542242.1:n.1902+704_1902+706del
XM_017029712.2:c.1569+4569_1569+4571del	XP_016885201.1:n.1569+4569_1569+4571del
NM_001367245.1:c.1902+704_1902+706del	NP_001354174.1:n.1902+704_1902+706del
NM_001367246.1:c.1719+704_1719+706del	NP_001354175.1:n.1719+704_1719+706del
NM_001367247.1:c.1572+4569_1572+4571del	NP_001354176.1:n.1572+4569_1572+4571del
NM_001367248.1:c.1602+4569_1602+4571del	NP_001354177.1:n.1602+4569_1602+4571del
NM_001367249.1:c.1569+4569_1569+4571del	NP_001354178.1:n.1569+4569_1569+4571del
NM_001367250.1:c.1569+4569_1569+4571del	NP_001354179.1:n.1569+4569_1569+4571del
NM_001367251.1:c.1386+4569_1386+4571del	NP_001354180.1:n.1386+4569_1386+4571del
NR_159803.1:n.2263+704_2263+706del
NR_159804.1:n.1648+4569_1648+4571del
NR_159805.1:n.1714+4569_1714+4571del
NR_159806.1:n.1866+704_1866+706del
NR_159807.1:n.1622+4569_1622+4571del
NR_159808.1:n.1826+4569_1826+4571del
NM_000328.3:c.1905+704_1905+706del	NP_000319.1:n.1905+704_1905+706del
NM_001034853.2:c.2609_2611del MANE Select	NP_001030025.1:p.Glu870del