Canonical Allele Identifier: CA2693438932

Gene: RPGR

Linked Data

• gnomAD v4: X-38286065-T-TTGG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38286066_38286067insGGT , CM000685.2:g.38286066_38286067insGGT	GRCh38
NC_000023.10:g.38145319_38145320insGGT , CM000685.1:g.38145319_38145320insGGT	GRCh37
NC_000023.9:g.38030263_38030264insGGT	NCBI36
NG_009553.1:g.46470_46471insCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494707.6:c.953+1799_953+1800insCCA
ENST00000642170.1:n.1826+4893_1826+4894insCCA
ENST00000642395.2:c.1905+1028_1905+1029insCCA	ENSP00000493468.2:n.1905+1028_1905+1029insCCA
ENST00000642739.1:c.1572+4893_1572+4894insCCA	ENSP00000493596.1:n.1572+4893_1572+4894insCCA
ENST00000644238.1:c.1386+4893_1386+4894insCCA	ENSP00000496728.1:n.1386+4893_1386+4894insCCA
ENST00000644337.1:c.1719+1028_1719+1029insCCA	ENSP00000494557.1:n.1719+1028_1719+1029insCCA
ENST00000645032.1:c.2933_2934insCCA MANE Select	ENSP00000495537.1:p.Glu978delinsAspGln
ENST00000645124.1:c.*101+1028_*101+1029insCCA	ENSP00000496446.1:n.*101+1028_*101+1029insCCA
ENST00000646020.1:c.*594+1028_*594+1029insCCA	ENSP00000494745.1:n.*594+1028_*594+1029insCCA
ENST00000318842.11:c.1905+1028_1905+1029insCCA	ENSP00000322219.6:n.1905+1028_1905+1029insCCA
ENST00000339363.7:c.2520+1028_2520+1029insCCA	ENSP00000343671.3:n.2520+1028_2520+1029insCCA
ENST00000378505.6:c.2933_2934insCCA	ENSP00000367766.2:p.Glu978delinsAspGln
ENST00000465127.1:c.172-380055_172-380054insGGT	ENSP00000417050.1:n.172-380055_172-380054insGGT
ENST00000474584.5:c.*37+4893_*37+4894insCCA	ENSP00000418926.1:n.*37+4893_*37+4894insCCA
ENST00000482855.5:c.1905+1028_1905+1029insCCA	ENSP00000419276.1:n.1905+1028_1905+1029insCCA
ENST00000494707.5:c.139+4893_139+4894insCCA
NM_000328.2:c.1905+1028_1905+1029insCCA	NP_000319.1:n.1905+1028_1905+1029insCCA
NM_001034853.1:c.2933_2934insCCA	NP_001030025.1:p.Glu978delinsAspGln
XM_005272633.1:c.1572+4893_1572+4894insCCA	XP_005272690.1:n.1572+4893_1572+4894insCCA
XM_011543940.1:c.1902+1028_1902+1029insCCA	XP_011542242.1:n.1902+1028_1902+1029insCCA
XM_005272633.3:c.1572+4893_1572+4894insCCA	XP_005272690.1:n.1572+4893_1572+4894insCCA
XM_011543940.3:c.1902+1028_1902+1029insCCA	XP_011542242.1:n.1902+1028_1902+1029insCCA
XM_017029712.2:c.1569+4893_1569+4894insCCA	XP_016885201.1:n.1569+4893_1569+4894insCCA
NM_001367245.1:c.1902+1028_1902+1029insCCA	NP_001354174.1:n.1902+1028_1902+1029insCCA
NM_001367246.1:c.1719+1028_1719+1029insCCA	NP_001354175.1:n.1719+1028_1719+1029insCCA
NM_001367247.1:c.1572+4893_1572+4894insCCA	NP_001354176.1:n.1572+4893_1572+4894insCCA
NM_001367248.1:c.1602+4893_1602+4894insCCA	NP_001354177.1:n.1602+4893_1602+4894insCCA
NM_001367249.1:c.1569+4893_1569+4894insCCA	NP_001354178.1:n.1569+4893_1569+4894insCCA
NM_001367250.1:c.1569+4893_1569+4894insCCA	NP_001354179.1:n.1569+4893_1569+4894insCCA
NM_001367251.1:c.1386+4893_1386+4894insCCA	NP_001354180.1:n.1386+4893_1386+4894insCCA
NR_159803.1:n.2263+1028_2263+1029insCCA
NR_159804.1:n.1648+4893_1648+4894insCCA
NR_159805.1:n.1714+4893_1714+4894insCCA
NR_159806.1:n.1866+1028_1866+1029insCCA
NR_159807.1:n.1622+4893_1622+4894insCCA
NR_159808.1:n.1826+4893_1826+4894insCCA
NM_000328.3:c.1905+1028_1905+1029insCCA	NP_000319.1:n.1905+1028_1905+1029insCCA
NM_001034853.2:c.2933_2934insCCA MANE Select	NP_001030025.1:p.Glu978delinsAspGln