Canonical Allele Identifier: CA2067787234

Gene: P2RX7

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121177339A= , CM000674.2:g.121177339A=	GRCh38
NC_000012.11:g.121615142A= , CM000674.1:g.121615142A=	GRCh37
NC_000012.10:g.120099525A=	NCBI36
NG_011471.2:g.49465A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328963.10:c.1081A= MANE Select	ENSP00000330696.6:p.Asn361=
ENST00000261826.10:c.*534A=	ENSP00000261826.6:n.*534A=
ENST00000328963.9:c.1081A=	ENSP00000330696.6:p.Asn361=
ENST00000535250.5:c.1165A=	ENSP00000442572.2:n.1165A=
ENST00000535600.2:c.898A=	ENSP00000442470.1:n.898A=
ENST00000537312.5:c.*852A=	ENSP00000438586.1:n.*852A=
ENST00000538011.5:c.1220A=	ENSP00000439247.1:n.1220A=
ENST00000539606.5:c.1304A=	ENSP00000445325.1:n.1304A=
ENST00000539695.5:n.1250A=
ENST00000541022.5:c.871A=	ENSP00000441230.1:n.871A=
ENST00000541564.5:c.944A=	ENSP00000443640.1:n.944A=
ENST00000541716.5:c.1092A=	ENSP00000437729.1:n.1092A=
NM_002562.5:c.1081A=	NP_002553.3:p.Asn361=
NR_033948.1:n.1447A=
NR_033949.1:n.1363A=
NR_033950.1:n.1324A=
NR_033951.1:n.1308A=
NR_033952.1:n.1235A=
NR_033953.1:n.1148A=
NR_033954.1:n.1127A=
NR_033955.1:n.1087A=
NR_033956.1:n.1014A=
XM_011538418.1:c.814A=	XP_011536720.1:p.Asn272=
XM_011538419.1:c.769A=	XP_011536721.1:p.Asn257=
XM_011538420.1:c.214A=	XP_011536722.1:p.Asn72=
XR_945459.1:n.190-14922T=
XR_945460.1:n.299-14922T=
XM_011538419.3:c.769A=	XP_011536721.1:p.Asn257=
XM_011538420.3:c.214A=	XP_011536722.1:p.Asn72=
XM_017019364.2:c.721A=	XP_016874853.1:p.Asn241=
XM_017019365.2:c.721A=	XP_016874854.1:p.Asn241=
XM_017019366.2:c.328A=	XP_016874855.1:p.Asn110=
XM_017019367.2:c.328A=	XP_016874856.1:p.Asn110=
XR_001749352.2:n.186+26159T=
XR_001749353.2:n.304-14922T=
XR_001749354.2:n.186+26159T=
XR_945459.3:n.187-14922T=
XR_945460.3:n.299-14922T=
NM_002562.6:c.1081A= MANE Select	NP_002553.3:p.Asn361=
NR_033948.2:n.1399A=
NR_033949.2:n.1315A=
NR_033950.2:n.1276A=
NR_033951.2:n.1260A=
NR_033952.2:n.1187A=
NR_033953.2:n.1091A=
NR_033954.2:n.1079A=
NR_033955.2:n.1039A=
NR_033956.2:n.966A=