Canonical Allele Identifier: CA2820486482

Gene: RPGR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38285824_38285825insACA , CM000685.2:g.38285824_38285825insACA	GRCh38
NC_000023.10:g.38145077_38145078insACA , CM000685.1:g.38145077_38145078insACA	GRCh37
NC_000023.9:g.38030021_38030022insACA	NCBI36
NG_009553.1:g.46711_46712insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494707.6:c.953+2040_953+2041insTGT
ENST00000642170.1:n.1826+5134_1826+5135insTGT
ENST00000642395.2:c.1905+1269_1905+1270insTGT	ENSP00000493468.2:n.1905+1269_1905+1270insTGT
ENST00000642739.1:c.1572+5134_1572+5135insTGT	ENSP00000493596.1:n.1572+5134_1572+5135insTGT
ENST00000644238.1:c.1386+5134_1386+5135insTGT	ENSP00000496728.1:n.1386+5134_1386+5135insTGT
ENST00000644337.1:c.1719+1269_1719+1270insTGT	ENSP00000494557.1:n.1719+1269_1719+1270insTGT
ENST00000645032.1:c.3174_3175insTGT MANE Select	ENSP00000495537.1:p.Asn1058_Arg1059insCys
ENST00000645124.1:c.*101+1269_*101+1270insTGT	ENSP00000496446.1:n.*101+1269_*101+1270insTGT
ENST00000646020.1:c.*594+1269_*594+1270insTGT	ENSP00000494745.1:n.*594+1269_*594+1270insTGT
ENST00000318842.11:c.1905+1269_1905+1270insTGT	ENSP00000322219.6:n.1905+1269_1905+1270insTGT
ENST00000339363.7:c.2520+1269_2520+1270insTGT	ENSP00000343671.3:n.2520+1269_2520+1270insTGT
ENST00000378505.6:c.3174_3175insTGT	ENSP00000367766.2:p.Asn1058_Arg1059insCys
ENST00000465127.1:c.172-380297_172-380296insACA	ENSP00000417050.1:n.172-380297_172-380296insACA
ENST00000474584.5:c.*37+5134_*37+5135insTGT	ENSP00000418926.1:n.*37+5134_*37+5135insTGT
ENST00000482855.5:c.1905+1269_1905+1270insTGT	ENSP00000419276.1:n.1905+1269_1905+1270insTGT
ENST00000494707.5:c.139+5134_139+5135insTGT
NM_000328.2:c.1905+1269_1905+1270insTGT	NP_000319.1:n.1905+1269_1905+1270insTGT
NM_001034853.1:c.3174_3175insTGT	NP_001030025.1:p.Asn1058_Arg1059insCys
XM_005272633.1:c.1572+5134_1572+5135insTGT	XP_005272690.1:n.1572+5134_1572+5135insTGT
XM_011543940.1:c.1902+1269_1902+1270insTGT	XP_011542242.1:n.1902+1269_1902+1270insTGT
XM_005272633.3:c.1572+5134_1572+5135insTGT	XP_005272690.1:n.1572+5134_1572+5135insTGT
XM_011543940.3:c.1902+1269_1902+1270insTGT	XP_011542242.1:n.1902+1269_1902+1270insTGT
XM_017029712.2:c.1569+5134_1569+5135insTGT	XP_016885201.1:n.1569+5134_1569+5135insTGT
NM_001367245.1:c.1902+1269_1902+1270insTGT	NP_001354174.1:n.1902+1269_1902+1270insTGT
NM_001367246.1:c.1719+1269_1719+1270insTGT	NP_001354175.1:n.1719+1269_1719+1270insTGT
NM_001367247.1:c.1572+5134_1572+5135insTGT	NP_001354176.1:n.1572+5134_1572+5135insTGT
NM_001367248.1:c.1602+5134_1602+5135insTGT	NP_001354177.1:n.1602+5134_1602+5135insTGT
NM_001367249.1:c.1569+5134_1569+5135insTGT	NP_001354178.1:n.1569+5134_1569+5135insTGT
NM_001367250.1:c.1569+5134_1569+5135insTGT	NP_001354179.1:n.1569+5134_1569+5135insTGT
NM_001367251.1:c.1386+5134_1386+5135insTGT	NP_001354180.1:n.1386+5134_1386+5135insTGT
NR_159803.1:n.2263+1269_2263+1270insTGT
NR_159804.1:n.1648+5134_1648+5135insTGT
NR_159805.1:n.1714+5134_1714+5135insTGT
NR_159806.1:n.1866+1269_1866+1270insTGT
NR_159807.1:n.1622+5134_1622+5135insTGT
NR_159808.1:n.1826+5134_1826+5135insTGT
NM_000328.3:c.1905+1269_1905+1270insTGT	NP_000319.1:n.1905+1269_1905+1270insTGT
NM_001034853.2:c.3174_3175insTGT MANE Select	NP_001030025.1:p.Asn1058_Arg1059insCys