Canonical Allele Identifier: CA2067787298

Gene: P2RX7

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121177376G= , CM000674.2:g.121177376G=	GRCh38
NC_000012.11:g.121615179G= , CM000674.1:g.121615179G=	GRCh37
NC_000012.10:g.120099562G=	NCBI36
NG_011471.2:g.49502G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328963.10:c.1118G= MANE Select	ENSP00000330696.6:p.Cys373=
ENST00000261826.10:c.*571G=	ENSP00000261826.6:n.*571G=
ENST00000328963.9:c.1118G=	ENSP00000330696.6:p.Cys373=
ENST00000535250.5:c.1202G=	ENSP00000442572.2:n.1202G=
ENST00000535600.2:c.935G=	ENSP00000442470.1:n.935G=
ENST00000537312.5:c.*889G=	ENSP00000438586.1:n.*889G=
ENST00000538011.5:c.1257G=	ENSP00000439247.1:n.1257G=
ENST00000539606.5:c.1341G=	ENSP00000445325.1:n.1341G=
ENST00000539695.5:n.1287G=
ENST00000541022.5:c.908G=	ENSP00000441230.1:n.908G=
ENST00000541564.5:c.981G=	ENSP00000443640.1:n.981G=
ENST00000541716.5:c.1129G=	ENSP00000437729.1:n.1129G=
NM_002562.5:c.1118G=	NP_002553.3:p.Cys373=
NR_033948.1:n.1484G=
NR_033949.1:n.1400G=
NR_033950.1:n.1361G=
NR_033951.1:n.1345G=
NR_033952.1:n.1272G=
NR_033953.1:n.1185G=
NR_033954.1:n.1164G=
NR_033955.1:n.1124G=
NR_033956.1:n.1051G=
XM_011538418.1:c.851G=	XP_011536720.1:p.Cys284=
XM_011538419.1:c.806G=	XP_011536721.1:p.Cys269=
XM_011538420.1:c.251G=	XP_011536722.1:p.Cys84=
XR_945459.1:n.190-14959C=
XR_945460.1:n.299-14959C=
XM_011538419.3:c.806G=	XP_011536721.1:p.Cys269=
XM_011538420.3:c.251G=	XP_011536722.1:p.Cys84=
XM_017019364.2:c.758G=	XP_016874853.1:p.Cys253=
XM_017019365.2:c.758G=	XP_016874854.1:p.Cys253=
XM_017019366.2:c.365G=	XP_016874855.1:p.Cys122=
XM_017019367.2:c.365G=	XP_016874856.1:p.Cys122=
XR_001749352.2:n.186+26122C=
XR_001749353.2:n.304-14959C=
XR_001749354.2:n.186+26122C=
XR_945459.3:n.187-14959C=
XR_945460.3:n.299-14959C=
NM_002562.6:c.1118G= MANE Select	NP_002553.3:p.Cys373=
NR_033948.2:n.1436G=
NR_033949.2:n.1352G=
NR_033950.2:n.1313G=
NR_033951.2:n.1297G=
NR_033952.2:n.1224G=
NR_033953.2:n.1128G=
NR_033954.2:n.1116G=
NR_033955.2:n.1076G=
NR_033956.2:n.1003G=