Canonical Allele Identifier: CA2820486518

Gene: RPGR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38285951_38285955del , CM000685.2:g.38285951_38285955del	GRCh38
NC_000023.10:g.38145204_38145208del , CM000685.1:g.38145204_38145208del	GRCh37
NC_000023.9:g.38030148_38030152del	NCBI36
NG_009553.1:g.46581_46585del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494707.6:c.953+1910_953+1914del
ENST00000642170.1:n.1826+5004_1826+5008del
ENST00000642395.2:c.1905+1139_1905+1143del	ENSP00000493468.2:n.1905+1139_1905+1143del
ENST00000642739.1:c.1572+5004_1572+5008del	ENSP00000493596.1:n.1572+5004_1572+5008del
ENST00000644238.1:c.1386+5004_1386+5008del	ENSP00000496728.1:n.1386+5004_1386+5008del
ENST00000644337.1:c.1719+1139_1719+1143del	ENSP00000494557.1:n.1719+1139_1719+1143del
ENST00000645032.1:c.3044_3048del MANE Select	ENSP00000495537.1:p.Glu1015GlyfsTer?
ENST00000645124.1:c.*101+1139_*101+1143del	ENSP00000496446.1:n.*101+1139_*101+1143del
ENST00000646020.1:c.*594+1139_*594+1143del	ENSP00000494745.1:n.*594+1139_*594+1143del
ENST00000318842.11:c.1905+1139_1905+1143del	ENSP00000322219.6:n.1905+1139_1905+1143del
ENST00000339363.7:c.2520+1139_2520+1143del	ENSP00000343671.3:n.2520+1139_2520+1143del
ENST00000378505.6:c.3044_3048del	ENSP00000367766.2:p.Glu1015GlyfsTer?
ENST00000465127.1:c.172-380170_172-380166del	ENSP00000417050.1:n.172-380170_172-380166del
ENST00000474584.5:c.*37+5004_*37+5008del	ENSP00000418926.1:n.*37+5004_*37+5008del
ENST00000482855.5:c.1905+1139_1905+1143del	ENSP00000419276.1:n.1905+1139_1905+1143del
ENST00000494707.5:c.139+5004_139+5008del
NM_000328.2:c.1905+1139_1905+1143del	NP_000319.1:n.1905+1139_1905+1143del
NM_001034853.1:c.3044_3048del	NP_001030025.1:p.Glu1015GlyfsTer?
XM_005272633.1:c.1572+5004_1572+5008del	XP_005272690.1:n.1572+5004_1572+5008del
XM_011543940.1:c.1902+1139_1902+1143del	XP_011542242.1:n.1902+1139_1902+1143del
XM_005272633.3:c.1572+5004_1572+5008del	XP_005272690.1:n.1572+5004_1572+5008del
XM_011543940.3:c.1902+1139_1902+1143del	XP_011542242.1:n.1902+1139_1902+1143del
XM_017029712.2:c.1569+5004_1569+5008del	XP_016885201.1:n.1569+5004_1569+5008del
NM_001367245.1:c.1902+1139_1902+1143del	NP_001354174.1:n.1902+1139_1902+1143del
NM_001367246.1:c.1719+1139_1719+1143del	NP_001354175.1:n.1719+1139_1719+1143del
NM_001367247.1:c.1572+5004_1572+5008del	NP_001354176.1:n.1572+5004_1572+5008del
NM_001367248.1:c.1602+5004_1602+5008del	NP_001354177.1:n.1602+5004_1602+5008del
NM_001367249.1:c.1569+5004_1569+5008del	NP_001354178.1:n.1569+5004_1569+5008del
NM_001367250.1:c.1569+5004_1569+5008del	NP_001354179.1:n.1569+5004_1569+5008del
NM_001367251.1:c.1386+5004_1386+5008del	NP_001354180.1:n.1386+5004_1386+5008del
NR_159803.1:n.2263+1139_2263+1143del
NR_159804.1:n.1648+5004_1648+5008del
NR_159805.1:n.1714+5004_1714+5008del
NR_159806.1:n.1866+1139_1866+1143del
NR_159807.1:n.1622+5004_1622+5008del
NR_159808.1:n.1826+5004_1826+5008del
NM_000328.3:c.1905+1139_1905+1143del	NP_000319.1:n.1905+1139_1905+1143del
NM_001034853.2:c.3044_3048del MANE Select	NP_001030025.1:p.Glu1015GlyfsTer?