Canonical Allele Identifier: CA2424848839

Gene: RPGR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38299087C= , CM000685.2:g.38299087C=	GRCh38
NC_000023.10:g.38158340C= , CM000685.1:g.38158340C=	GRCh37
NC_000023.9:g.38043284C=	NCBI36
NG_009553.1:g.33449G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494707.6:c.318G=
ENST00000642170.1:n.1368G=
ENST00000642395.2:c.1114G=	ENSP00000493468.2:p.Ala372=
ENST00000642558.1:c.1021G=	ENSP00000496427.1:p.Ala341=
ENST00000642739.1:c.1114G=	ENSP00000493596.1:p.Ala372=
ENST00000644238.1:c.1060-1635G=	ENSP00000496728.1:n.1060-1635G=
ENST00000644337.1:c.1060-1635G=	ENSP00000494557.1:n.1060-1635G=
ENST00000645032.1:c.1114G= MANE Select	ENSP00000495537.1:p.Ala372=
ENST00000645124.1:c.1114G=	ENSP00000496446.1:p.Ala372=
ENST00000646020.1:c.1174G=	ENSP00000494745.1:p.Ala392=
ENST00000318842.11:c.1114G=	ENSP00000322219.6:p.Ala372=
ENST00000339363.7:c.1114G=	ENSP00000343671.3:p.Ala372=
ENST00000378505.6:c.1114G=	ENSP00000367766.2:p.Ala372=
ENST00000464437.1:c.180G=
ENST00000465127.1:c.172-367034C=	ENSP00000417050.1:n.172-367034C=
ENST00000474584.5:c.1114G=	ENSP00000418926.1:p.Ala372=
ENST00000482855.5:c.1114G=	ENSP00000419276.1:p.Ala372=
ENST00000494841.1:n.377G=
NM_000328.2:c.1114G=	NP_000319.1:p.Ala372=
NM_001034853.1:c.1114G=	NP_001030025.1:p.Ala372=
XM_005272633.1:c.1114G=	XP_005272690.1:p.Ala372=
XM_011543940.1:c.1111G=	XP_011542242.1:p.Ala371=
XM_005272633.3:c.1114G=	XP_005272690.1:p.Ala372=
XM_011543940.3:c.1111G=	XP_011542242.1:p.Ala371=
XM_017029712.2:c.1111G=	XP_016885201.1:p.Ala371=
NM_001367245.1:c.1111G=	NP_001354174.1:p.Ala371=
NM_001367246.1:c.1060-1635G=	NP_001354175.1:n.1060-1635G=
NM_001367247.1:c.1114G=	NP_001354176.1:p.Ala372=
NM_001367248.1:c.1144G=	NP_001354177.1:p.Ala382=
NM_001367249.1:c.1111G=	NP_001354178.1:p.Ala371=
NM_001367250.1:c.1111G=	NP_001354179.1:p.Ala371=
NM_001367251.1:c.1060-1635G=	NP_001354180.1:n.1060-1635G=
NR_159803.1:n.1316G=
NR_159804.1:n.1165G=
NR_159805.1:n.1256G=
NR_159806.1:n.1256G=
NR_159807.1:n.1256G=
NR_159808.1:n.1368G=
NM_000328.3:c.1114G=	NP_000319.1:p.Ala372=
NM_001034853.2:c.1114G= MANE Select	NP_001030025.1:p.Ala372=