Canonical Allele Identifier: CA2693439043

Gene: RPGR

Linked Data

• gnomAD v4: X-38286216-CCTTCCTCTCCTTCCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38286218_38286232del , CM000685.2:g.38286218_38286232del	GRCh38
NC_000023.10:g.38145471_38145485del , CM000685.1:g.38145471_38145485del	GRCh37
NC_000023.9:g.38030415_38030429del	NCBI36
NG_009553.1:g.46305_46319del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494707.6:c.953+1634_953+1648del
ENST00000642170.1:n.1826+4728_1826+4742del
ENST00000642395.2:c.1905+863_1905+877del	ENSP00000493468.2:n.1905+863_1905+877del
ENST00000642739.1:c.1572+4728_1572+4742del	ENSP00000493596.1:n.1572+4728_1572+4742del
ENST00000644238.1:c.1386+4728_1386+4742del	ENSP00000496728.1:n.1386+4728_1386+4742del
ENST00000644337.1:c.1719+863_1719+877del	ENSP00000494557.1:n.1719+863_1719+877del
ENST00000645032.1:c.2768_2782del MANE Select	ENSP00000495537.1:p.Glu923_Glu927del
ENST00000645124.1:c.*101+863_*101+877del	ENSP00000496446.1:n.*101+863_*101+877del
ENST00000646020.1:c.*594+863_*594+877del	ENSP00000494745.1:n.*594+863_*594+877del
ENST00000318842.11:c.1905+863_1905+877del	ENSP00000322219.6:n.1905+863_1905+877del
ENST00000339363.7:c.2520+863_2520+877del	ENSP00000343671.3:n.2520+863_2520+877del
ENST00000378505.6:c.2768_2782del	ENSP00000367766.2:p.Glu923_Glu927del
ENST00000465127.1:c.172-379903_172-379889del	ENSP00000417050.1:n.172-379903_172-379889del
ENST00000474584.5:c.*37+4728_*37+4742del	ENSP00000418926.1:n.*37+4728_*37+4742del
ENST00000482855.5:c.1905+863_1905+877del	ENSP00000419276.1:n.1905+863_1905+877del
ENST00000494707.5:c.139+4728_139+4742del
NM_000328.2:c.1905+863_1905+877del	NP_000319.1:n.1905+863_1905+877del
NM_001034853.1:c.2768_2782del	NP_001030025.1:p.Glu923_Glu927del
XM_005272633.1:c.1572+4728_1572+4742del	XP_005272690.1:n.1572+4728_1572+4742del
XM_011543940.1:c.1902+863_1902+877del	XP_011542242.1:n.1902+863_1902+877del
XM_005272633.3:c.1572+4728_1572+4742del	XP_005272690.1:n.1572+4728_1572+4742del
XM_011543940.3:c.1902+863_1902+877del	XP_011542242.1:n.1902+863_1902+877del
XM_017029712.2:c.1569+4728_1569+4742del	XP_016885201.1:n.1569+4728_1569+4742del
NM_001367245.1:c.1902+863_1902+877del	NP_001354174.1:n.1902+863_1902+877del
NM_001367246.1:c.1719+863_1719+877del	NP_001354175.1:n.1719+863_1719+877del
NM_001367247.1:c.1572+4728_1572+4742del	NP_001354176.1:n.1572+4728_1572+4742del
NM_001367248.1:c.1602+4728_1602+4742del	NP_001354177.1:n.1602+4728_1602+4742del
NM_001367249.1:c.1569+4728_1569+4742del	NP_001354178.1:n.1569+4728_1569+4742del
NM_001367250.1:c.1569+4728_1569+4742del	NP_001354179.1:n.1569+4728_1569+4742del
NM_001367251.1:c.1386+4728_1386+4742del	NP_001354180.1:n.1386+4728_1386+4742del
NR_159803.1:n.2263+863_2263+877del
NR_159804.1:n.1648+4728_1648+4742del
NR_159805.1:n.1714+4728_1714+4742del
NR_159806.1:n.1866+863_1866+877del
NR_159807.1:n.1622+4728_1622+4742del
NR_159808.1:n.1826+4728_1826+4742del
NM_000328.3:c.1905+863_1905+877del	NP_000319.1:n.1905+863_1905+877del
NM_001034853.2:c.2768_2782del MANE Select	NP_001030025.1:p.Glu923_Glu927del