Canonical Allele Identifier: CA412739851

Gene: RPGR

Linked Data

• MyVariant Identifiers: chrX:g.38158280G>T (hg19) ; chrX:g.38299027G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38299027G>T , CM000685.2:g.38299027G>T	GRCh38
NC_000023.10:g.38158280G>T , CM000685.1:g.38158280G>T	GRCh37
NC_000023.9:g.38043224G>T	NCBI36
NG_009553.1:g.33509C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000494707.6:c.378C>A
ENST00000642170.1:n.1428C>A
ENST00000642395.2:c.1174C>A	ENSP00000493468.2:p.Pro392Thr
ENST00000642558.1:c.1081C>A	ENSP00000496427.1:p.Pro361Thr
ENST00000642739.1:c.1174C>A	ENSP00000493596.1:p.Pro392Thr
ENST00000644238.1:c.1060-1575C>A	ENSP00000496728.1:n.1060-1575C>A
ENST00000644337.1:c.1060-1575C>A	ENSP00000494557.1:n.1060-1575C>A
ENST00000645032.1:c.1174C>A MANE Select	ENSP00000495537.1:p.Pro392Thr
ENST00000645124.1:c.1174C>A	ENSP00000496446.1:p.Pro392Thr
ENST00000646020.1:c.1234C>A	ENSP00000494745.1:p.Pro412Thr
ENST00000318842.11:c.1174C>A	ENSP00000322219.6:p.Pro392Thr
ENST00000339363.7:c.1174C>A	ENSP00000343671.3:p.Pro392Thr
ENST00000378505.6:c.1174C>A	ENSP00000367766.2:p.Pro392Thr
ENST00000464437.1:c.240C>A
ENST00000465127.1:c.172-367094G>T	ENSP00000417050.1:n.172-367094G>T
ENST00000474584.5:c.1174C>A	ENSP00000418926.1:p.Pro392Thr
ENST00000482855.5:c.1174C>A	ENSP00000419276.1:p.Pro392Thr
ENST00000494841.1:n.437C>A
NM_000328.2:c.1174C>A	NP_000319.1:p.Pro392Thr
NM_001034853.1:c.1174C>A	NP_001030025.1:p.Pro392Thr
XM_005272633.1:c.1174C>A	XP_005272690.1:p.Pro392Thr
XM_011543940.1:c.1171C>A	XP_011542242.1:p.Pro391Thr
XM_005272633.3:c.1174C>A	XP_005272690.1:p.Pro392Thr
XM_011543940.3:c.1171C>A	XP_011542242.1:p.Pro391Thr
XM_017029712.2:c.1171C>A	XP_016885201.1:p.Pro391Thr
NM_001367245.1:c.1171C>A	NP_001354174.1:p.Pro391Thr
NM_001367246.1:c.1060-1575C>A	NP_001354175.1:n.1060-1575C>A
NM_001367247.1:c.1174C>A	NP_001354176.1:p.Pro392Thr
NM_001367248.1:c.1204C>A	NP_001354177.1:p.Pro402Thr
NM_001367249.1:c.1171C>A	NP_001354178.1:p.Pro391Thr
NM_001367250.1:c.1171C>A	NP_001354179.1:p.Pro391Thr
NM_001367251.1:c.1060-1575C>A	NP_001354180.1:n.1060-1575C>A
NR_159803.1:n.1376C>A
NR_159804.1:n.1225C>A
NR_159805.1:n.1316C>A
NR_159806.1:n.1316C>A
NR_159807.1:n.1316C>A
NR_159808.1:n.1428C>A
NM_000328.3:c.1174C>A	NP_000319.1:p.Pro392Thr
NM_001034853.2:c.1174C>A MANE Select	NP_001030025.1:p.Pro392Thr