Canonical Allele Identifier: CA2693439071

Gene: RPGR

Linked Data

• gnomAD v4: X-38286377-TCCTTCCTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38286380_38286387del , CM000685.2:g.38286380_38286387del	GRCh38
NC_000023.10:g.38145633_38145640del , CM000685.1:g.38145633_38145640del	GRCh37
NC_000023.9:g.38030577_38030584del	NCBI36
NG_009553.1:g.46151_46158del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494707.6:c.953+1480_953+1487del
ENST00000642170.1:n.1826+4574_1826+4581del
ENST00000642395.2:c.1905+709_1905+716del	ENSP00000493468.2:n.1905+709_1905+716del
ENST00000642739.1:c.1572+4574_1572+4581del	ENSP00000493596.1:n.1572+4574_1572+4581del
ENST00000644238.1:c.1386+4574_1386+4581del	ENSP00000496728.1:n.1386+4574_1386+4581del
ENST00000644337.1:c.1719+709_1719+716del	ENSP00000494557.1:n.1719+709_1719+716del
ENST00000645032.1:c.2614_2621del MANE Select	ENSP00000495537.1:p.Glu872ArgfsTer?
ENST00000645124.1:c.*101+709_*101+716del	ENSP00000496446.1:n.*101+709_*101+716del
ENST00000646020.1:c.*594+709_*594+716del	ENSP00000494745.1:n.*594+709_*594+716del
ENST00000318842.11:c.1905+709_1905+716del	ENSP00000322219.6:n.1905+709_1905+716del
ENST00000339363.7:c.2520+709_2520+716del	ENSP00000343671.3:n.2520+709_2520+716del
ENST00000378505.6:c.2614_2621del	ENSP00000367766.2:p.Glu872ArgfsTer?
ENST00000465127.1:c.172-379741_172-379734del	ENSP00000417050.1:n.172-379741_172-379734del
ENST00000474584.5:c.*37+4574_*37+4581del	ENSP00000418926.1:n.*37+4574_*37+4581del
ENST00000482855.5:c.1905+709_1905+716del	ENSP00000419276.1:n.1905+709_1905+716del
ENST00000494707.5:c.139+4574_139+4581del
NM_000328.2:c.1905+709_1905+716del	NP_000319.1:n.1905+709_1905+716del
NM_001034853.1:c.2614_2621del	NP_001030025.1:p.Glu872ArgfsTer?
XM_005272633.1:c.1572+4574_1572+4581del	XP_005272690.1:n.1572+4574_1572+4581del
XM_011543940.1:c.1902+709_1902+716del	XP_011542242.1:n.1902+709_1902+716del
XM_005272633.3:c.1572+4574_1572+4581del	XP_005272690.1:n.1572+4574_1572+4581del
XM_011543940.3:c.1902+709_1902+716del	XP_011542242.1:n.1902+709_1902+716del
XM_017029712.2:c.1569+4574_1569+4581del	XP_016885201.1:n.1569+4574_1569+4581del
NM_001367245.1:c.1902+709_1902+716del	NP_001354174.1:n.1902+709_1902+716del
NM_001367246.1:c.1719+709_1719+716del	NP_001354175.1:n.1719+709_1719+716del
NM_001367247.1:c.1572+4574_1572+4581del	NP_001354176.1:n.1572+4574_1572+4581del
NM_001367248.1:c.1602+4574_1602+4581del	NP_001354177.1:n.1602+4574_1602+4581del
NM_001367249.1:c.1569+4574_1569+4581del	NP_001354178.1:n.1569+4574_1569+4581del
NM_001367250.1:c.1569+4574_1569+4581del	NP_001354179.1:n.1569+4574_1569+4581del
NM_001367251.1:c.1386+4574_1386+4581del	NP_001354180.1:n.1386+4574_1386+4581del
NR_159803.1:n.2263+709_2263+716del
NR_159804.1:n.1648+4574_1648+4581del
NR_159805.1:n.1714+4574_1714+4581del
NR_159806.1:n.1866+709_1866+716del
NR_159807.1:n.1622+4574_1622+4581del
NR_159808.1:n.1826+4574_1826+4581del
NM_000328.3:c.1905+709_1905+716del	NP_000319.1:n.1905+709_1905+716del
NM_001034853.2:c.2614_2621del MANE Select	NP_001030025.1:p.Glu872ArgfsTer?