Canonical Allele Identifier: CA2067787331

Gene: P2RX7

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121177397_121177398delinsAC , CM000674.2:g.121177397_121177398delinsAC	GRCh38
NC_000012.11:g.121615200_121615201delinsAC , CM000674.1:g.121615200_121615201delinsAC	GRCh37
NC_000012.10:g.120099583_120099584delinsAC	NCBI36
NG_011471.2:g.49523_49524delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328963.10:c.1139_1140delinsAC MANE Select	ENSP00000330696.6:p.Asn380=
ENST00000261826.10:c.*592_*593delinsAC	ENSP00000261826.6:n.*592_*593delinsAC
ENST00000328963.9:c.1139_1140delinsAC	ENSP00000330696.6:p.Asn380=
ENST00000535250.5:c.1223_1224delinsAC	ENSP00000442572.2:n.1223_1224delinsAC
ENST00000535600.2:c.956_957delinsAC	ENSP00000442470.1:n.956_957delinsAC
ENST00000537312.5:c.*910_*911delinsAC	ENSP00000438586.1:n.*910_*911delinsAC
ENST00000538011.5:c.1278_1279delinsAC	ENSP00000439247.1:n.1278_1279delinsAC
ENST00000539606.5:c.1362_1363delinsAC	ENSP00000445325.1:n.1362_1363delinsAC
ENST00000539695.5:n.1308_1309delinsAC
ENST00000541022.5:c.929_930delinsAC	ENSP00000441230.1:n.929_930delinsAC
ENST00000541564.5:c.1002_1003delinsAC	ENSP00000443640.1:n.1002_1003delinsAC
ENST00000541716.5:c.1150_1151delinsAC	ENSP00000437729.1:n.1150_1151delinsAC
NM_002562.5:c.1139_1140delinsAC	NP_002553.3:p.Asn380=
NR_033948.1:n.1505_1506delinsAC
NR_033949.1:n.1421_1422delinsAC
NR_033950.1:n.1382_1383delinsAC
NR_033951.1:n.1366_1367delinsAC
NR_033952.1:n.1293_1294delinsAC
NR_033953.1:n.1206_1207delinsAC
NR_033954.1:n.1185_1186delinsAC
NR_033955.1:n.1145_1146delinsAC
NR_033956.1:n.1072_1073delinsAC
XM_011538418.1:c.872_873delinsAC	XP_011536720.1:p.Asn291=
XM_011538419.1:c.827_828delinsAC	XP_011536721.1:p.Asn276=
XM_011538420.1:c.272_273delinsAC	XP_011536722.1:p.Asn91=
XR_945459.1:n.190-14981_190-14980delinsGT
XR_945460.1:n.299-14981_299-14980delinsGT
XM_011538419.3:c.827_828delinsAC	XP_011536721.1:p.Asn276=
XM_011538420.3:c.272_273delinsAC	XP_011536722.1:p.Asn91=
XM_017019364.2:c.779_780delinsAC	XP_016874853.1:p.Asn260=
XM_017019365.2:c.779_780delinsAC	XP_016874854.1:p.Asn260=
XM_017019366.2:c.386_387delinsAC	XP_016874855.1:p.Asn129=
XM_017019367.2:c.386_387delinsAC	XP_016874856.1:p.Asn129=
XR_001749352.2:n.186+26100_186+26101delinsGT
XR_001749353.2:n.304-14981_304-14980delinsGT
XR_001749354.2:n.186+26100_186+26101delinsGT
XR_945459.3:n.187-14981_187-14980delinsGT
XR_945460.3:n.299-14981_299-14980delinsGT
NM_002562.6:c.1139_1140delinsAC MANE Select	NP_002553.3:p.Asn380=
NR_033948.2:n.1457_1458delinsAC
NR_033949.2:n.1373_1374delinsAC
NR_033950.2:n.1334_1335delinsAC
NR_033951.2:n.1318_1319delinsAC
NR_033952.2:n.1245_1246delinsAC
NR_033953.2:n.1149_1150delinsAC
NR_033954.2:n.1137_1138delinsAC
NR_033955.2:n.1097_1098delinsAC
NR_033956.2:n.1024_1025delinsAC