Canonical Allele Identifier: CA2067768569

Gene: P2RX7

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121133028C= , CM000674.2:g.121133028C=	GRCh38
NC_000012.11:g.121570831C= , CM000674.1:g.121570831C=	GRCh37
NC_000012.10:g.120055214C=	NCBI36
NG_011471.2:g.5154C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328963.10:c.58C= MANE Select	ENSP00000330696.6:p.Arg20=
ENST00000261826.10:c.58C=	ENSP00000261826.6:p.Arg20=
ENST00000328963.9:c.58C=	ENSP00000330696.6:p.Arg20=
ENST00000535250.5:c.58C=	ENSP00000442572.2:p.Arg20=
ENST00000535600.2:c.58C=	ENSP00000442470.1:p.Arg20=
ENST00000535928.5:c.58C=	ENSP00000439961.1:p.Arg20=
ENST00000537312.5:c.58C=	ENSP00000438586.1:p.Arg20=
ENST00000538011.5:c.58C=	ENSP00000439247.1:p.Arg20=
ENST00000539606.5:c.58C=	ENSP00000445325.1:p.Arg20=
ENST00000539695.5:n.127C=
ENST00000541022.5:c.58C=	ENSP00000441230.1:p.Arg20=
ENST00000541564.5:c.58C=	ENSP00000443640.1:p.Arg20=
ENST00000541716.5:c.58C=	ENSP00000437729.1:p.Arg20=
ENST00000545434.5:c.58C=	ENSP00000445564.1:p.Arg20=
NM_002562.5:c.58C=	NP_002553.3:p.Arg20=
NR_033948.1:n.201C=
NR_033949.1:n.201C=
NR_033950.1:n.201C=
NR_033951.1:n.201C=
NR_033952.1:n.201C=
NR_033953.1:n.210C=
NR_033954.1:n.201C=
NR_033955.1:n.201C=
NR_033956.1:n.201C=
XM_011538418.1:c.58C=	XP_011536720.1:p.Arg20=
XM_011538419.1:c.-86C=	XP_011536721.1:n.-86C=
XM_011538420.1:c.-504C=	XP_011536722.1:n.-504C=
XM_011538419.3:c.-86C=	XP_011536721.1:n.-86C=
XM_011538420.3:c.-504C=	XP_011536722.1:n.-504C=
XM_017019364.2:c.-456C=	XP_016874853.1:n.-456C=
XM_017019365.2:c.-287C=	XP_016874854.1:n.-287C=
XM_017019366.2:c.-623C=	XP_016874855.1:n.-623C=
XM_017019367.2:c.-454C=	XP_016874856.1:n.-454C=
XR_001749352.2:n.187-6187G=
XR_001749354.2:n.187-6187G=
NM_002562.6:c.58C= MANE Select	NP_002553.3:p.Arg20=
NR_033948.2:n.153C=
NR_033949.2:n.153C=
NR_033950.2:n.153C=
NR_033951.2:n.153C=
NR_033952.2:n.153C=
NR_033953.2:n.153C=
NR_033954.2:n.153C=
NR_033955.2:n.153C=
NR_033956.2:n.153C=