Canonical Allele Identifier: CA412729485

Gene: RPGR

Linked Data

• ClinVar Variation Id: 1983577
• ClinVar RCV Id: RCV002770342
• dbSNP Id: rs1555961470
• gnomAD v3: X-38286092-T-TTCC
• gnomAD v4: X-38286092-T-TTCC
• MyVariant Identifiers: chrX:g.38145345_38145346insTCC (hg19) ; chrX:g.38286092_38286093insTCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38286095_38286097dup , CM000685.2:g.38286095_38286097dup	GRCh38
NC_000023.10:g.38145348_38145350dup , CM000685.1:g.38145348_38145350dup	GRCh37
NC_000023.9:g.38030292_38030294dup	NCBI36
NG_009553.1:g.46441_46443dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494707.6:c.953+1770_953+1772dup
ENST00000642170.1:n.1826+4864_1826+4866dup
ENST00000642395.2:c.1905+999_1905+1001dup	ENSP00000493468.2:n.1905+999_1905+1001dup
ENST00000642739.1:c.1572+4864_1572+4866dup	ENSP00000493596.1:n.1572+4864_1572+4866dup
ENST00000644238.1:c.1386+4864_1386+4866dup	ENSP00000496728.1:n.1386+4864_1386+4866dup
ENST00000644337.1:c.1719+999_1719+1001dup	ENSP00000494557.1:n.1719+999_1719+1001dup
ENST00000645032.1:c.2904_2906dup MANE Select	ENSP00000495537.1:p.Glu969_Gly970insGlu
ENST00000645124.1:c.*101+999_*101+1001dup	ENSP00000496446.1:n.*101+999_*101+1001dup
ENST00000646020.1:c.*594+999_*594+1001dup	ENSP00000494745.1:n.*594+999_*594+1001dup
ENST00000318842.11:c.1905+999_1905+1001dup	ENSP00000322219.6:n.1905+999_1905+1001dup
ENST00000339363.7:c.2520+999_2520+1001dup	ENSP00000343671.3:n.2520+999_2520+1001dup
ENST00000378505.6:c.2904_2906dup	ENSP00000367766.2:p.Glu969_Gly970insGlu
ENST00000465127.1:c.172-380026_172-380024dup	ENSP00000417050.1:n.172-380026_172-380024dup
ENST00000474584.5:c.*37+4864_*37+4866dup	ENSP00000418926.1:n.*37+4864_*37+4866dup
ENST00000482855.5:c.1905+999_1905+1001dup	ENSP00000419276.1:n.1905+999_1905+1001dup
ENST00000494707.5:c.139+4864_139+4866dup
NM_000328.2:c.1905+999_1905+1001dup	NP_000319.1:n.1905+999_1905+1001dup
NM_001034853.1:c.2904_2906dup	NP_001030025.1:p.Glu969_Gly970insGlu
XM_005272633.1:c.1572+4864_1572+4866dup	XP_005272690.1:n.1572+4864_1572+4866dup
XM_011543940.1:c.1902+999_1902+1001dup	XP_011542242.1:n.1902+999_1902+1001dup
XM_005272633.3:c.1572+4864_1572+4866dup	XP_005272690.1:n.1572+4864_1572+4866dup
XM_011543940.3:c.1902+999_1902+1001dup	XP_011542242.1:n.1902+999_1902+1001dup
XM_017029712.2:c.1569+4864_1569+4866dup	XP_016885201.1:n.1569+4864_1569+4866dup
NM_001367245.1:c.1902+999_1902+1001dup	NP_001354174.1:n.1902+999_1902+1001dup
NM_001367246.1:c.1719+999_1719+1001dup	NP_001354175.1:n.1719+999_1719+1001dup
NM_001367247.1:c.1572+4864_1572+4866dup	NP_001354176.1:n.1572+4864_1572+4866dup
NM_001367248.1:c.1602+4864_1602+4866dup	NP_001354177.1:n.1602+4864_1602+4866dup
NM_001367249.1:c.1569+4864_1569+4866dup	NP_001354178.1:n.1569+4864_1569+4866dup
NM_001367250.1:c.1569+4864_1569+4866dup	NP_001354179.1:n.1569+4864_1569+4866dup
NM_001367251.1:c.1386+4864_1386+4866dup	NP_001354180.1:n.1386+4864_1386+4866dup
NR_159803.1:n.2263+999_2263+1001dup
NR_159804.1:n.1648+4864_1648+4866dup
NR_159805.1:n.1714+4864_1714+4866dup
NR_159806.1:n.1866+999_1866+1001dup
NR_159807.1:n.1622+4864_1622+4866dup
NR_159808.1:n.1826+4864_1826+4866dup
NM_000328.3:c.1905+999_1905+1001dup	NP_000319.1:n.1905+999_1905+1001dup
NM_001034853.2:c.2904_2906dup MANE Select	NP_001030025.1:p.Glu969_Gly970insGlu