Canonical Allele Identifier: CA2693438954

Gene: RPGR

Linked Data

• gnomAD v4: X-38286106-C-CCCCTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38286111_38286112insTCCCTT , CM000685.2:g.38286111_38286112insTCCCTT	GRCh38
NC_000023.10:g.38145364_38145365insTCCCTT , CM000685.1:g.38145364_38145365insTCCCTT	GRCh37
NC_000023.9:g.38030308_38030309insTCCCTT	NCBI36
NG_009553.1:g.46429_46430insAAAGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494707.6:c.953+1758_953+1759insAAAGGG
ENST00000642170.1:n.1826+4852_1826+4853insAAAGGG
ENST00000642395.2:c.1905+987_1905+988insAAAGGG	ENSP00000493468.2:n.1905+987_1905+988insAAAGGG
ENST00000642739.1:c.1572+4852_1572+4853insAAAGGG	ENSP00000493596.1:n.1572+4852_1572+4853insAAAGGG
ENST00000644238.1:c.1386+4852_1386+4853insAAAGGG	ENSP00000496728.1:n.1386+4852_1386+4853insAAAGGG
ENST00000644337.1:c.1719+987_1719+988insAAAGGG	ENSP00000494557.1:n.1719+987_1719+988insAAAGGG
ENST00000645032.1:c.2892_2893insAAAGGG MANE Select	ENSP00000495537.1:p.Gly964_Glu965insLysGly
ENST00000645124.1:c.*101+987_*101+988insAAAGGG	ENSP00000496446.1:n.*101+987_*101+988insAAAGGG
ENST00000646020.1:c.*594+987_*594+988insAAAGGG	ENSP00000494745.1:n.*594+987_*594+988insAAAGGG
ENST00000318842.11:c.1905+987_1905+988insAAAGGG	ENSP00000322219.6:n.1905+987_1905+988insAAAGGG
ENST00000339363.7:c.2520+987_2520+988insAAAGGG	ENSP00000343671.3:n.2520+987_2520+988insAAAGGG
ENST00000378505.6:c.2892_2893insAAAGGG	ENSP00000367766.2:p.Gly964_Glu965insLysGly
ENST00000465127.1:c.172-380010_172-380009insTCCCTT	ENSP00000417050.1:n.172-380010_172-380009insTCCCTT
ENST00000474584.5:c.*37+4852_*37+4853insAAAGGG	ENSP00000418926.1:n.*37+4852_*37+4853insAAAGGG
ENST00000482855.5:c.1905+987_1905+988insAAAGGG	ENSP00000419276.1:n.1905+987_1905+988insAAAGGG
ENST00000494707.5:c.139+4852_139+4853insAAAGGG
NM_000328.2:c.1905+987_1905+988insAAAGGG	NP_000319.1:n.1905+987_1905+988insAAAGGG
NM_001034853.1:c.2892_2893insAAAGGG	NP_001030025.1:p.Gly964_Glu965insLysGly
XM_005272633.1:c.1572+4852_1572+4853insAAAGGG	XP_005272690.1:n.1572+4852_1572+4853insAAAGGG
XM_011543940.1:c.1902+987_1902+988insAAAGGG	XP_011542242.1:n.1902+987_1902+988insAAAGGG
XM_005272633.3:c.1572+4852_1572+4853insAAAGGG	XP_005272690.1:n.1572+4852_1572+4853insAAAGGG
XM_011543940.3:c.1902+987_1902+988insAAAGGG	XP_011542242.1:n.1902+987_1902+988insAAAGGG
XM_017029712.2:c.1569+4852_1569+4853insAAAGGG	XP_016885201.1:n.1569+4852_1569+4853insAAAGGG
NM_001367245.1:c.1902+987_1902+988insAAAGGG	NP_001354174.1:n.1902+987_1902+988insAAAGGG
NM_001367246.1:c.1719+987_1719+988insAAAGGG	NP_001354175.1:n.1719+987_1719+988insAAAGGG
NM_001367247.1:c.1572+4852_1572+4853insAAAGGG	NP_001354176.1:n.1572+4852_1572+4853insAAAGGG
NM_001367248.1:c.1602+4852_1602+4853insAAAGGG	NP_001354177.1:n.1602+4852_1602+4853insAAAGGG
NM_001367249.1:c.1569+4852_1569+4853insAAAGGG	NP_001354178.1:n.1569+4852_1569+4853insAAAGGG
NM_001367250.1:c.1569+4852_1569+4853insAAAGGG	NP_001354179.1:n.1569+4852_1569+4853insAAAGGG
NM_001367251.1:c.1386+4852_1386+4853insAAAGGG	NP_001354180.1:n.1386+4852_1386+4853insAAAGGG
NR_159803.1:n.2263+987_2263+988insAAAGGG
NR_159804.1:n.1648+4852_1648+4853insAAAGGG
NR_159805.1:n.1714+4852_1714+4853insAAAGGG
NR_159806.1:n.1866+987_1866+988insAAAGGG
NR_159807.1:n.1622+4852_1622+4853insAAAGGG
NR_159808.1:n.1826+4852_1826+4853insAAAGGG
NM_000328.3:c.1905+987_1905+988insAAAGGG	NP_000319.1:n.1905+987_1905+988insAAAGGG
NM_001034853.2:c.2892_2893insAAAGGG MANE Select	NP_001030025.1:p.Gly964_Glu965insLysGly