Canonical Allele Identifier: CA412729442

Gene: RPGR

Linked Data

• dbSNP Id: rs1219943432
• gnomAD v3: X-38286074-CTCCCCTTCCCCT-C
• gnomAD v4: X-38286074-CTCCCCTTCCCCT-C
• COSMIC: COSM4722536
• MyVariant Identifiers: chrX:g.38145328_38145339del (hg19) ; chrX:g.38286076_38286087del (hg38) ; chrX:g.38286075_38286086del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38286077_38286088del , CM000685.2:g.38286077_38286088del	GRCh38
NC_000023.10:g.38145330_38145341del , CM000685.1:g.38145330_38145341del	GRCh37
NC_000023.9:g.38030274_38030285del	NCBI36
NG_009553.1:g.46450_46461del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494707.6:c.953+1779_953+1790del
ENST00000642170.1:n.1826+4873_1826+4884del
ENST00000642395.2:c.1905+1008_1905+1019del	ENSP00000493468.2:n.1905+1008_1905+1019del
ENST00000642739.1:c.1572+4873_1572+4884del	ENSP00000493596.1:n.1572+4873_1572+4884del
ENST00000644238.1:c.1386+4873_1386+4884del	ENSP00000496728.1:n.1386+4873_1386+4884del
ENST00000644337.1:c.1719+1008_1719+1019del	ENSP00000494557.1:n.1719+1008_1719+1019del
ENST00000645032.1:c.2913_2924del MANE Select	ENSP00000495537.1:p.Gly972_Glu975del
ENST00000645124.1:c.*101+1008_*101+1019del	ENSP00000496446.1:n.*101+1008_*101+1019del
ENST00000646020.1:c.*594+1008_*594+1019del	ENSP00000494745.1:n.*594+1008_*594+1019del
ENST00000318842.11:c.1905+1008_1905+1019del	ENSP00000322219.6:n.1905+1008_1905+1019del
ENST00000339363.7:c.2520+1008_2520+1019del	ENSP00000343671.3:n.2520+1008_2520+1019del
ENST00000378505.6:c.2913_2924del	ENSP00000367766.2:p.Gly972_Glu975del
ENST00000465127.1:c.172-380044_172-380033del	ENSP00000417050.1:n.172-380044_172-380033del
ENST00000474584.5:c.*37+4873_*37+4884del	ENSP00000418926.1:n.*37+4873_*37+4884del
ENST00000482855.5:c.1905+1008_1905+1019del	ENSP00000419276.1:n.1905+1008_1905+1019del
ENST00000494707.5:c.139+4873_139+4884del
NM_000328.2:c.1905+1008_1905+1019del	NP_000319.1:n.1905+1008_1905+1019del
NM_001034853.1:c.2913_2924del	NP_001030025.1:p.Gly972_Glu975del
XM_005272633.1:c.1572+4873_1572+4884del	XP_005272690.1:n.1572+4873_1572+4884del
XM_011543940.1:c.1902+1008_1902+1019del	XP_011542242.1:n.1902+1008_1902+1019del
XM_005272633.3:c.1572+4873_1572+4884del	XP_005272690.1:n.1572+4873_1572+4884del
XM_011543940.3:c.1902+1008_1902+1019del	XP_011542242.1:n.1902+1008_1902+1019del
XM_017029712.2:c.1569+4873_1569+4884del	XP_016885201.1:n.1569+4873_1569+4884del
NM_001367245.1:c.1902+1008_1902+1019del	NP_001354174.1:n.1902+1008_1902+1019del
NM_001367246.1:c.1719+1008_1719+1019del	NP_001354175.1:n.1719+1008_1719+1019del
NM_001367247.1:c.1572+4873_1572+4884del	NP_001354176.1:n.1572+4873_1572+4884del
NM_001367248.1:c.1602+4873_1602+4884del	NP_001354177.1:n.1602+4873_1602+4884del
NM_001367249.1:c.1569+4873_1569+4884del	NP_001354178.1:n.1569+4873_1569+4884del
NM_001367250.1:c.1569+4873_1569+4884del	NP_001354179.1:n.1569+4873_1569+4884del
NM_001367251.1:c.1386+4873_1386+4884del	NP_001354180.1:n.1386+4873_1386+4884del
NR_159803.1:n.2263+1008_2263+1019del
NR_159804.1:n.1648+4873_1648+4884del
NR_159805.1:n.1714+4873_1714+4884del
NR_159806.1:n.1866+1008_1866+1019del
NR_159807.1:n.1622+4873_1622+4884del
NR_159808.1:n.1826+4873_1826+4884del
NM_000328.3:c.1905+1008_1905+1019del	NP_000319.1:n.1905+1008_1905+1019del
NM_001034853.2:c.2913_2924del MANE Select	NP_001030025.1:p.Gly972_Glu975del