Canonical Allele Identifier: CA640957200

Gene: RPGR

Linked Data

• dbSNP Id: rs1307994442
• gnomAD v2: X-38145467-CTCCTTCCTCTCCTTCCTCCTCCCCTTT-C
• gnomAD v3: X-38286214-CTCCTTCCTCTCCTTCCTCCTCCCCTTT-C
• gnomAD v4: X-38286214-CTCCTTCCTCTCCTTCCTCCTCCCCTTT-C
• MyVariant Identifiers: chrX:g.38145468_38145494del (hg19) ; chrX:g.38286215_38286241del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38286215_38286241del , CM000685.2:g.38286215_38286241del	GRCh38
NC_000023.10:g.38145468_38145494del , CM000685.1:g.38145468_38145494del	GRCh37
NC_000023.9:g.38030412_38030438del	NCBI36
NG_009553.1:g.46295_46321del

Transcript Alleles

HGVS	Amino-acid change
ENST00000494707.6:c.953+1624_953+1650del
ENST00000642170.1:n.1826+4718_1826+4744del
ENST00000642395.2:c.1905+853_1905+879del	ENSP00000493468.2:n.1905+853_1905+879del
ENST00000642739.1:c.1572+4718_1572+4744del	ENSP00000493596.1:n.1572+4718_1572+4744de...
ENST00000644238.1:c.1386+4718_1386+4744del	ENSP00000496728.1:n.1386+4718_1386+4744de...
ENST00000644337.1:c.1719+853_1719+879del	ENSP00000494557.1:n.1719+853_1719+879del
ENST00000645032.1:c.2758_2784del MANE Select	ENSP00000495537.1:p.Lys920_Gly928del
ENST00000645124.1:c.*101+853_*101+879del	ENSP00000496446.1:n.*101+853_*101+879del
ENST00000646020.1:c.*594+853_*594+879del	ENSP00000494745.1:n.*594+853_*594+879del
ENST00000318842.11:c.1905+853_1905+879del	ENSP00000322219.6:n.1905+853_1905+879del
ENST00000339363.7:c.2520+853_2520+879del	ENSP00000343671.3:n.2520+853_2520+879del
ENST00000378505.6:c.2758_2784del	ENSP00000367766.2:p.Lys920_Gly928del
ENST00000465127.1:c.172-379906_172-379880del	ENSP00000417050.1:n.172-379906_172-379880...
ENST00000474584.5:c.*37+4718_*37+4744del	ENSP00000418926.1:n.*37+4718_*37+4744del
ENST00000482855.5:c.1905+853_1905+879del	ENSP00000419276.1:n.1905+853_1905+879del
ENST00000494707.5:c.139+4718_139+4744del
NM_000328.2:c.1905+853_1905+879del	NP_000319.1:n.1905+853_1905+879del
NM_001034853.1:c.2758_2784del	NP_001030025.1:p.Lys920_Gly928del
XM_005272633.1:c.1572+4718_1572+4744del	XP_005272690.1:n.1572+4718_1572+4744del
XM_011543940.1:c.1902+853_1902+879del	XP_011542242.1:n.1902+853_1902+879del
XM_005272633.3:c.1572+4718_1572+4744del	XP_005272690.1:n.1572+4718_1572+4744del
XM_011543940.3:c.1902+853_1902+879del	XP_011542242.1:n.1902+853_1902+879del
XM_017029712.2:c.1569+4718_1569+4744del	XP_016885201.1:n.1569+4718_1569+4744del
NM_001367245.1:c.1902+853_1902+879del	NP_001354174.1:n.1902+853_1902+879del
NM_001367246.1:c.1719+853_1719+879del	NP_001354175.1:n.1719+853_1719+879del
NM_001367247.1:c.1572+4718_1572+4744del	NP_001354176.1:n.1572+4718_1572+4744del
NM_001367248.1:c.1602+4718_1602+4744del	NP_001354177.1:n.1602+4718_1602+4744del
NM_001367249.1:c.1569+4718_1569+4744del	NP_001354178.1:n.1569+4718_1569+4744del
NM_001367250.1:c.1569+4718_1569+4744del	NP_001354179.1:n.1569+4718_1569+4744del
NM_001367251.1:c.1386+4718_1386+4744del	NP_001354180.1:n.1386+4718_1386+4744del
NR_159803.1:n.2263+853_2263+879del
NR_159804.1:n.1648+4718_1648+4744del
NR_159805.1:n.1714+4718_1714+4744del
NR_159806.1:n.1866+853_1866+879del
NR_159807.1:n.1622+4718_1622+4744del
NR_159808.1:n.1826+4718_1826+4744del
NM_000328.3:c.1905+853_1905+879del	NP_000319.1:n.1905+853_1905+879del
NM_001034853.2:c.2758_2784del MANE Select	NP_001030025.1:p.Lys920_Gly928del