Canonical Allele Identifier: CA2067787376

Gene: P2RX7

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121177419G= , CM000674.2:g.121177419G=	GRCh38
NC_000012.11:g.121615222G= , CM000674.1:g.121615222G=	GRCh37
NC_000012.10:g.120099605G=	NCBI36
NG_011471.2:g.49545G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328963.10:c.1161G= MANE Select	ENSP00000330696.6:p.Lys387=
ENST00000261826.10:c.*614G=	ENSP00000261826.6:n.*614G=
ENST00000328963.9:c.1161G=	ENSP00000330696.6:p.Lys387=
ENST00000535250.5:c.1245G=	ENSP00000442572.2:n.1245G=
ENST00000535600.2:c.978G=	ENSP00000442470.1:n.978G=
ENST00000537312.5:c.*932G=	ENSP00000438586.1:n.*932G=
ENST00000538011.5:c.1300G=	ENSP00000439247.1:n.1300G=
ENST00000539606.5:c.1384G=	ENSP00000445325.1:n.1384G=
ENST00000539695.5:n.1330G=
ENST00000541022.5:c.951G=	ENSP00000441230.1:n.951G=
ENST00000541564.5:c.1024G=	ENSP00000443640.1:n.1024G=
ENST00000541716.5:c.1172G=	ENSP00000437729.1:n.1172G=
NM_002562.5:c.1161G=	NP_002553.3:p.Lys387=
NR_033948.1:n.1527G=
NR_033949.1:n.1443G=
NR_033950.1:n.1404G=
NR_033951.1:n.1388G=
NR_033952.1:n.1315G=
NR_033953.1:n.1228G=
NR_033954.1:n.1207G=
NR_033955.1:n.1167G=
NR_033956.1:n.1094G=
XM_011538418.1:c.894G=	XP_011536720.1:p.Lys298=
XM_011538419.1:c.849G=	XP_011536721.1:p.Lys283=
XM_011538420.1:c.294G=	XP_011536722.1:p.Lys98=
XR_945459.1:n.190-15002C=
XR_945460.1:n.299-15002C=
XM_011538419.3:c.849G=	XP_011536721.1:p.Lys283=
XM_011538420.3:c.294G=	XP_011536722.1:p.Lys98=
XM_017019364.2:c.801G=	XP_016874853.1:p.Lys267=
XM_017019365.2:c.801G=	XP_016874854.1:p.Lys267=
XM_017019366.2:c.408G=	XP_016874855.1:p.Lys136=
XM_017019367.2:c.408G=	XP_016874856.1:p.Lys136=
XR_001749352.2:n.186+26079C=
XR_001749353.2:n.304-15002C=
XR_001749354.2:n.186+26079C=
XR_945459.3:n.187-15002C=
XR_945460.3:n.299-15002C=
NM_002562.6:c.1161G= MANE Select	NP_002553.3:p.Lys387=
NR_033948.2:n.1479G=
NR_033949.2:n.1395G=
NR_033950.2:n.1356G=
NR_033951.2:n.1340G=
NR_033952.2:n.1267G=
NR_033953.2:n.1171G=
NR_033954.2:n.1159G=
NR_033955.2:n.1119G=
NR_033956.2:n.1046G=