Canonical Allele Identifier: CA10385291

Gene: RPGR

Linked Data

• ClinVar Variation Id: 257193
• ClinVar RCV Id: RCV000248693 ; RCV000828504 ; RCV001510189 ; RCV003888659
• dbSNP Id: rs5917557
• ExAC: X:38145911 C / T
• gnomAD v2: X-38145911-C-T
• gnomAD v3: X-38286658-C-T
• gnomAD v4: X-38286658-C-T
• MyVariant Identifiers: chrX:g.38145911C>T (hg19) ; chrX:g.38286658C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38286658C>T , CM000685.2:g.38286658C>T	GRCh38
NC_000023.10:g.38145911C>T , CM000685.1:g.38145911C>T	GRCh37
NC_000023.9:g.38030855C>T	NCBI36
NG_009553.1:g.45878G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000494707.6:c.953+1207G>A
ENST00000642170.1:n.1826+4301G>A
ENST00000642395.2:c.1905+436G>A	ENSP00000493468.2:n.1905+436G>A
ENST00000642739.1:c.1572+4301G>A	ENSP00000493596.1:n.1572+4301G>A
ENST00000644238.1:c.1386+4301G>A	ENSP00000496728.1:n.1386+4301G>A
ENST00000644337.1:c.1719+436G>A	ENSP00000494557.1:n.1719+436G>A
ENST00000645032.1:c.2341G>A MANE Select	ENSP00000495537.1:p.Ala781Thr
ENST00000645124.1:c.*101+436G>A	ENSP00000496446.1:n.*101+436G>A
ENST00000646020.1:c.*594+436G>A	ENSP00000494745.1:n.*594+436G>A
ENST00000318842.11:c.1905+436G>A	ENSP00000322219.6:n.1905+436G>A
ENST00000339363.7:c.2520+436G>A	ENSP00000343671.3:n.2520+436G>A
ENST00000378505.6:c.2341G>A	ENSP00000367766.2:p.Ala781Thr
ENST00000465127.1:c.172-379463C>T	ENSP00000417050.1:n.172-379463C>T
ENST00000474584.5:c.*37+4301G>A	ENSP00000418926.1:n.*37+4301G>A
ENST00000482855.5:c.1905+436G>A	ENSP00000419276.1:n.1905+436G>A
ENST00000494707.5:c.139+4301G>A
NM_000328.2:c.1905+436G>A	NP_000319.1:n.1905+436G>A
NM_001034853.1:c.2341G>A	NP_001030025.1:p.Ala781Thr
XM_005272633.1:c.1572+4301G>A	XP_005272690.1:n.1572+4301G>A
XM_011543940.1:c.1902+436G>A	XP_011542242.1:n.1902+436G>A
XM_005272633.3:c.1572+4301G>A	XP_005272690.1:n.1572+4301G>A
XM_011543940.3:c.1902+436G>A	XP_011542242.1:n.1902+436G>A
XM_017029712.2:c.1569+4301G>A	XP_016885201.1:n.1569+4301G>A
NM_001367245.1:c.1902+436G>A	NP_001354174.1:n.1902+436G>A
NM_001367246.1:c.1719+436G>A	NP_001354175.1:n.1719+436G>A
NM_001367247.1:c.1572+4301G>A	NP_001354176.1:n.1572+4301G>A
NM_001367248.1:c.1602+4301G>A	NP_001354177.1:n.1602+4301G>A
NM_001367249.1:c.1569+4301G>A	NP_001354178.1:n.1569+4301G>A
NM_001367250.1:c.1569+4301G>A	NP_001354179.1:n.1569+4301G>A
NM_001367251.1:c.1386+4301G>A	NP_001354180.1:n.1386+4301G>A
NR_159803.1:n.2263+436G>A
NR_159804.1:n.1648+4301G>A
NR_159805.1:n.1714+4301G>A
NR_159806.1:n.1866+436G>A
NR_159807.1:n.1622+4301G>A
NR_159808.1:n.1826+4301G>A
NM_000328.3:c.1905+436G>A	NP_000319.1:n.1905+436G>A
NM_001034853.2:c.2341G>A MANE Select	NP_001030025.1:p.Ala781Thr