Canonical Allele Identifier: CA2067787260

Gene: P2RX7

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121177353C= , CM000674.2:g.121177353C=	GRCh38
NC_000012.11:g.121615156C= , CM000674.1:g.121615156C=	GRCh37
NC_000012.10:g.120099539C=	NCBI36
NG_011471.2:g.49479C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328963.10:c.1095C= MANE Select	ENSP00000330696.6:p.Ser365=
ENST00000261826.10:c.*548C=	ENSP00000261826.6:n.*548C=
ENST00000328963.9:c.1095C=	ENSP00000330696.6:p.Ser365=
ENST00000535250.5:c.1179C=	ENSP00000442572.2:n.1179C=
ENST00000535600.2:c.912C=	ENSP00000442470.1:n.912C=
ENST00000537312.5:c.*866C=	ENSP00000438586.1:n.*866C=
ENST00000538011.5:c.1234C=	ENSP00000439247.1:n.1234C=
ENST00000539606.5:c.1318C=	ENSP00000445325.1:n.1318C=
ENST00000539695.5:n.1264C=
ENST00000541022.5:c.885C=	ENSP00000441230.1:n.885C=
ENST00000541564.5:c.958C=	ENSP00000443640.1:n.958C=
ENST00000541716.5:c.1106C=	ENSP00000437729.1:n.1106C=
NM_002562.5:c.1095C=	NP_002553.3:p.Ser365=
NR_033948.1:n.1461C=
NR_033949.1:n.1377C=
NR_033950.1:n.1338C=
NR_033951.1:n.1322C=
NR_033952.1:n.1249C=
NR_033953.1:n.1162C=
NR_033954.1:n.1141C=
NR_033955.1:n.1101C=
NR_033956.1:n.1028C=
XM_011538418.1:c.828C=	XP_011536720.1:p.Ser276=
XM_011538419.1:c.783C=	XP_011536721.1:p.Ser261=
XM_011538420.1:c.228C=	XP_011536722.1:p.Ser76=
XR_945459.1:n.190-14936G=
XR_945460.1:n.299-14936G=
XM_011538419.3:c.783C=	XP_011536721.1:p.Ser261=
XM_011538420.3:c.228C=	XP_011536722.1:p.Ser76=
XM_017019364.2:c.735C=	XP_016874853.1:p.Ser245=
XM_017019365.2:c.735C=	XP_016874854.1:p.Ser245=
XM_017019366.2:c.342C=	XP_016874855.1:p.Ser114=
XM_017019367.2:c.342C=	XP_016874856.1:p.Ser114=
XR_001749352.2:n.186+26145G=
XR_001749353.2:n.304-14936G=
XR_001749354.2:n.186+26145G=
XR_945459.3:n.187-14936G=
XR_945460.3:n.299-14936G=
NM_002562.6:c.1095C= MANE Select	NP_002553.3:p.Ser365=
NR_033948.2:n.1413C=
NR_033949.2:n.1329C=
NR_033950.2:n.1290C=
NR_033951.2:n.1274C=
NR_033952.2:n.1201C=
NR_033953.2:n.1105C=
NR_033954.2:n.1093C=
NR_033955.2:n.1053C=
NR_033956.2:n.980C=