Canonical Allele Identifier: CA10385237

Gene: RPGR

Linked Data

• dbSNP Id: rs758486646
• ExAC: X:38145350 CTT / C
• gnomAD v4: X-38286097-CTT-C
• MyVariant Identifiers: chrX:g.38145351_38145352del (hg19) ; chrX:g.38286098_38286099del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38286098_38286099del , CM000685.2:g.38286098_38286099del	GRCh38
NC_000023.10:g.38145351_38145352del , CM000685.1:g.38145351_38145352del	GRCh37
NC_000023.9:g.38030295_38030296del	NCBI36
NG_009553.1:g.46437_46438del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494707.6:c.953+1766_953+1767del
ENST00000642170.1:n.1826+4860_1826+4861del
ENST00000642395.2:c.1905+995_1905+996del	ENSP00000493468.2:n.1905+995_1905+996del
ENST00000642739.1:c.1572+4860_1572+4861del	ENSP00000493596.1:n.1572+4860_1572+4861del
ENST00000644238.1:c.1386+4860_1386+4861del	ENSP00000496728.1:n.1386+4860_1386+4861del
ENST00000644337.1:c.1719+995_1719+996del	ENSP00000494557.1:n.1719+995_1719+996del
ENST00000645032.1:c.2900_2901del MANE Select	ENSP00000495537.1:p.Glu967GlyfsTer?
ENST00000645124.1:c.*101+995_*101+996del	ENSP00000496446.1:n.*101+995_*101+996del
ENST00000646020.1:c.*594+995_*594+996del	ENSP00000494745.1:n.*594+995_*594+996del
ENST00000318842.11:c.1905+995_1905+996del	ENSP00000322219.6:n.1905+995_1905+996del
ENST00000339363.7:c.2520+995_2520+996del	ENSP00000343671.3:n.2520+995_2520+996del
ENST00000378505.6:c.2900_2901del	ENSP00000367766.2:p.Glu967GlyfsTer?
ENST00000465127.1:c.172-380023_172-380022del	ENSP00000417050.1:n.172-380023_172-380022del
ENST00000474584.5:c.*37+4860_*37+4861del	ENSP00000418926.1:n.*37+4860_*37+4861del
ENST00000482855.5:c.1905+995_1905+996del	ENSP00000419276.1:n.1905+995_1905+996del
ENST00000494707.5:c.139+4860_139+4861del
NM_000328.2:c.1905+995_1905+996del	NP_000319.1:n.1905+995_1905+996del
NM_001034853.1:c.2900_2901del	NP_001030025.1:p.Glu967GlyfsTer?
XM_005272633.1:c.1572+4860_1572+4861del	XP_005272690.1:n.1572+4860_1572+4861del
XM_011543940.1:c.1902+995_1902+996del	XP_011542242.1:n.1902+995_1902+996del
XM_005272633.3:c.1572+4860_1572+4861del	XP_005272690.1:n.1572+4860_1572+4861del
XM_011543940.3:c.1902+995_1902+996del	XP_011542242.1:n.1902+995_1902+996del
XM_017029712.2:c.1569+4860_1569+4861del	XP_016885201.1:n.1569+4860_1569+4861del
NM_001367245.1:c.1902+995_1902+996del	NP_001354174.1:n.1902+995_1902+996del
NM_001367246.1:c.1719+995_1719+996del	NP_001354175.1:n.1719+995_1719+996del
NM_001367247.1:c.1572+4860_1572+4861del	NP_001354176.1:n.1572+4860_1572+4861del
NM_001367248.1:c.1602+4860_1602+4861del	NP_001354177.1:n.1602+4860_1602+4861del
NM_001367249.1:c.1569+4860_1569+4861del	NP_001354178.1:n.1569+4860_1569+4861del
NM_001367250.1:c.1569+4860_1569+4861del	NP_001354179.1:n.1569+4860_1569+4861del
NM_001367251.1:c.1386+4860_1386+4861del	NP_001354180.1:n.1386+4860_1386+4861del
NR_159803.1:n.2263+995_2263+996del
NR_159804.1:n.1648+4860_1648+4861del
NR_159805.1:n.1714+4860_1714+4861del
NR_159806.1:n.1866+995_1866+996del
NR_159807.1:n.1622+4860_1622+4861del
NR_159808.1:n.1826+4860_1826+4861del
NM_000328.3:c.1905+995_1905+996del	NP_000319.1:n.1905+995_1905+996del
NM_001034853.2:c.2900_2901del MANE Select	NP_001030025.1:p.Glu967GlyfsTer?