Canonical Allele Identifier: CA226349

Gene: RPGR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38297419_38297437del , CM000685.2:g.38297419_38297437del	GRCh38
NC_000023.10:g.38156672_38156690del , CM000685.1:g.38156672_38156690del	GRCh37
NC_000023.9:g.38041616_38041634del	NCBI36
NG_009553.1:g.35099_35117del

Transcript Alleles

HGVS	Amino-acid Change
NM_001034853.2:c.1261_1279del MANE Select	NP_001030025.1:p.Ser421HisfsTer5
ENST00000645032.1:c.1261_1279del MANE Select	ENSP00000495537.1:p.Ser421HisfsTer5
NM_000328.2:c.1261_1279del	NP_000319.1:p.Ser421HisfsTer5
NM_000328.3:c.1261_1279del	NP_000319.1:p.Ser421HisfsTer5
NM_001034853.1:c.1261_1279del	NP_001030025.1:p.Ser421HisfsTer5
NM_001367245.1:c.1258_1276del	NP_001354174.1:p.Ser420HisfsTer5
NM_001367246.1:c.1075_1093del	NP_001354175.1:p.Ser359HisfsTer5
NM_001367247.1:c.1261_1279del	NP_001354176.1:p.Ser421HisfsTer5
NM_001367248.1:c.1291_1309del	NP_001354177.1:p.Ser431HisfsTer5
NM_001367249.1:c.1258_1276del	NP_001354178.1:p.Ser420HisfsTer5
NM_001367250.1:c.1258_1276del	NP_001354179.1:p.Ser420HisfsTer5
NM_001367251.1:c.1075_1093del	NP_001354180.1:p.Ser359HisfsTer5
NR_159803.1:n.1463_1481del
NR_159804.1:n.1337_1355del
NR_159805.1:n.1403_1421del
NR_159806.1:n.1403_1421del
NR_159807.1:n.1403_1421del
NR_159808.1:n.1515_1533del
ENST00000318842.11:c.1261_1279del	ENSP00000322219.6:p.Ser421HisfsTer5
ENST00000339363.7:c.1261_1279del	ENSP00000343671.3:p.Ser421HisfsTer5
ENST00000378505.6:c.1261_1279del	ENSP00000367766.2:p.Ser421HisfsTer5
ENST00000465127.1:c.172-368702_172-368684del	ENSP00000417050.1:n.172-368702_172-368684del
ENST00000474584.5:c.1261_1279del	ENSP00000418926.1:p.Ser421HisfsTer5
ENST00000482855.5:c.1261_1279del	ENSP00000419276.1:p.Ser421HisfsTer5
ENST00000494707.6:c.465_483del
ENST00000494841.1:n.524_542del
ENST00000642170.1:n.1515_1533del
ENST00000642395.2:c.1261_1279del	ENSP00000493468.2:p.Ser421HisfsTer5
ENST00000642739.1:c.1261_1279del	ENSP00000493596.1:p.Ser421HisfsTer5
ENST00000644238.1:c.1075_1093del	ENSP00000496728.1:p.Ser359HisfsTer5
ENST00000644337.1:c.1075_1093del	ENSP00000494557.1:p.Ser359HisfsTer5
ENST00000645124.1:c.1261_1279del	ENSP00000496446.1:p.Ser421HisfsTer5
ENST00000646020.1:c.1321_1339del	ENSP00000494745.1:p.Ser441HisfsTer5
XM_005272633.1:c.1261_1279del	XP_005272690.1:p.Ser421HisfsTer5
XM_005272633.3:c.1261_1279del	XP_005272690.1:p.Ser421HisfsTer5
XM_011543940.1:c.1258_1276del	XP_011542242.1:p.Ser420HisfsTer5
XM_011543940.3:c.1258_1276del	XP_011542242.1:p.Ser420HisfsTer5
XM_017029712.2:c.1258_1276del	XP_016885201.1:p.Ser420HisfsTer5