Canonical Allele Identifier: CA2693439083

Gene: RPGR

Linked Data

• gnomAD v4: X-38286435-T-TCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38286436_38286437insCCC , CM000685.2:g.38286436_38286437insCCC	GRCh38
NC_000023.10:g.38145689_38145690insCCC , CM000685.1:g.38145689_38145690insCCC	GRCh37
NC_000023.9:g.38030633_38030634insCCC	NCBI36
NG_009553.1:g.46100_46101insGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494707.6:c.953+1429_953+1430insGGG
ENST00000642170.1:n.1826+4523_1826+4524insGGG
ENST00000642395.2:c.1905+658_1905+659insGGG	ENSP00000493468.2:n.1905+658_1905+659insGGG
ENST00000642739.1:c.1572+4523_1572+4524insGGG	ENSP00000493596.1:n.1572+4523_1572+4524insGGG
ENST00000644238.1:c.1386+4523_1386+4524insGGG	ENSP00000496728.1:n.1386+4523_1386+4524insGGG
ENST00000644337.1:c.1719+658_1719+659insGGG	ENSP00000494557.1:n.1719+658_1719+659insGGG
ENST00000645032.1:c.2563_2564insGGG MANE Select	ENSP00000495537.1:p.Gly854_Glu855insGly
ENST00000645124.1:c.*101+658_*101+659insGGG	ENSP00000496446.1:n.*101+658_*101+659insGGG
ENST00000646020.1:c.*594+658_*594+659insGGG	ENSP00000494745.1:n.*594+658_*594+659insGGG
ENST00000318842.11:c.1905+658_1905+659insGGG	ENSP00000322219.6:n.1905+658_1905+659insGGG
ENST00000339363.7:c.2520+658_2520+659insGGG	ENSP00000343671.3:n.2520+658_2520+659insGGG
ENST00000378505.6:c.2563_2564insGGG	ENSP00000367766.2:p.Gly854_Glu855insGly
ENST00000465127.1:c.172-379685_172-379684insCCC	ENSP00000417050.1:n.172-379685_172-379684insCCC
ENST00000474584.5:c.*37+4523_*37+4524insGGG	ENSP00000418926.1:n.*37+4523_*37+4524insGGG
ENST00000482855.5:c.1905+658_1905+659insGGG	ENSP00000419276.1:n.1905+658_1905+659insGGG
ENST00000494707.5:c.139+4523_139+4524insGGG
NM_000328.2:c.1905+658_1905+659insGGG	NP_000319.1:n.1905+658_1905+659insGGG
NM_001034853.1:c.2563_2564insGGG	NP_001030025.1:p.Gly854_Glu855insGly
XM_005272633.1:c.1572+4523_1572+4524insGGG	XP_005272690.1:n.1572+4523_1572+4524insGGG
XM_011543940.1:c.1902+658_1902+659insGGG	XP_011542242.1:n.1902+658_1902+659insGGG
XM_005272633.3:c.1572+4523_1572+4524insGGG	XP_005272690.1:n.1572+4523_1572+4524insGGG
XM_011543940.3:c.1902+658_1902+659insGGG	XP_011542242.1:n.1902+658_1902+659insGGG
XM_017029712.2:c.1569+4523_1569+4524insGGG	XP_016885201.1:n.1569+4523_1569+4524insGGG
NM_001367245.1:c.1902+658_1902+659insGGG	NP_001354174.1:n.1902+658_1902+659insGGG
NM_001367246.1:c.1719+658_1719+659insGGG	NP_001354175.1:n.1719+658_1719+659insGGG
NM_001367247.1:c.1572+4523_1572+4524insGGG	NP_001354176.1:n.1572+4523_1572+4524insGGG
NM_001367248.1:c.1602+4523_1602+4524insGGG	NP_001354177.1:n.1602+4523_1602+4524insGGG
NM_001367249.1:c.1569+4523_1569+4524insGGG	NP_001354178.1:n.1569+4523_1569+4524insGGG
NM_001367250.1:c.1569+4523_1569+4524insGGG	NP_001354179.1:n.1569+4523_1569+4524insGGG
NM_001367251.1:c.1386+4523_1386+4524insGGG	NP_001354180.1:n.1386+4523_1386+4524insGGG
NR_159803.1:n.2263+658_2263+659insGGG
NR_159804.1:n.1648+4523_1648+4524insGGG
NR_159805.1:n.1714+4523_1714+4524insGGG
NR_159806.1:n.1866+658_1866+659insGGG
NR_159807.1:n.1622+4523_1622+4524insGGG
NR_159808.1:n.1826+4523_1826+4524insGGG
NM_000328.3:c.1905+658_1905+659insGGG	NP_000319.1:n.1905+658_1905+659insGGG
NM_001034853.2:c.2563_2564insGGG MANE Select	NP_001030025.1:p.Gly854_Glu855insGly