Canonical Allele Identifier: CA2067787240

Gene: P2RX7

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121177344C= , CM000674.2:g.121177344C=	GRCh38
NC_000012.11:g.121615147C= , CM000674.1:g.121615147C=	GRCh37
NC_000012.10:g.120099530C=	NCBI36
NG_011471.2:g.49470C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328963.10:c.1086C= MANE Select	ENSP00000330696.6:p.Cys362=
ENST00000261826.10:c.*539C=	ENSP00000261826.6:n.*539C=
ENST00000328963.9:c.1086C=	ENSP00000330696.6:p.Cys362=
ENST00000535250.5:c.1170C=	ENSP00000442572.2:n.1170C=
ENST00000535600.2:c.903C=	ENSP00000442470.1:n.903C=
ENST00000537312.5:c.*857C=	ENSP00000438586.1:n.*857C=
ENST00000538011.5:c.1225C=	ENSP00000439247.1:n.1225C=
ENST00000539606.5:c.1309C=	ENSP00000445325.1:n.1309C=
ENST00000539695.5:n.1255C=
ENST00000541022.5:c.876C=	ENSP00000441230.1:n.876C=
ENST00000541564.5:c.949C=	ENSP00000443640.1:n.949C=
ENST00000541716.5:c.1097C=	ENSP00000437729.1:n.1097C=
NM_002562.5:c.1086C=	NP_002553.3:p.Cys362=
NR_033948.1:n.1452C=
NR_033949.1:n.1368C=
NR_033950.1:n.1329C=
NR_033951.1:n.1313C=
NR_033952.1:n.1240C=
NR_033953.1:n.1153C=
NR_033954.1:n.1132C=
NR_033955.1:n.1092C=
NR_033956.1:n.1019C=
XM_011538418.1:c.819C=	XP_011536720.1:p.Cys273=
XM_011538419.1:c.774C=	XP_011536721.1:p.Cys258=
XM_011538420.1:c.219C=	XP_011536722.1:p.Cys73=
XR_945459.1:n.190-14927G=
XR_945460.1:n.299-14927G=
XM_011538419.3:c.774C=	XP_011536721.1:p.Cys258=
XM_011538420.3:c.219C=	XP_011536722.1:p.Cys73=
XM_017019364.2:c.726C=	XP_016874853.1:p.Cys242=
XM_017019365.2:c.726C=	XP_016874854.1:p.Cys242=
XM_017019366.2:c.333C=	XP_016874855.1:p.Cys111=
XM_017019367.2:c.333C=	XP_016874856.1:p.Cys111=
XR_001749352.2:n.186+26154G=
XR_001749353.2:n.304-14927G=
XR_001749354.2:n.186+26154G=
XR_945459.3:n.187-14927G=
XR_945460.3:n.299-14927G=
NM_002562.6:c.1086C= MANE Select	NP_002553.3:p.Cys362=
NR_033948.2:n.1404C=
NR_033949.2:n.1320C=
NR_033950.2:n.1281C=
NR_033951.2:n.1265C=
NR_033952.2:n.1192C=
NR_033953.2:n.1096C=
NR_033954.2:n.1084C=
NR_033955.2:n.1044C=
NR_033956.2:n.971C=