Canonical Allele Identifier: CA2067768519

Gene: P2RX7

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121132995G= , CM000674.2:g.121132995G=	GRCh38
NC_000012.11:g.121570798G= , CM000674.1:g.121570798G=	GRCh37
NC_000012.10:g.120055181G=	NCBI36
NG_011471.2:g.5121G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328963.10:c.25G= MANE Select	ENSP00000330696.6:p.Asp9=
ENST00000261826.10:c.25G=	ENSP00000261826.6:p.Asp9=
ENST00000328963.9:c.25G=	ENSP00000330696.6:p.Asp9=
ENST00000535250.5:c.25G=	ENSP00000442572.2:p.Asp9=
ENST00000535600.2:c.25G=	ENSP00000442470.1:p.Asp9=
ENST00000535928.5:c.25G=	ENSP00000439961.1:p.Asp9=
ENST00000537312.5:c.25G=	ENSP00000438586.1:p.Asp9=
ENST00000538011.5:c.25G=	ENSP00000439247.1:p.Asp9=
ENST00000539606.5:c.25G=	ENSP00000445325.1:p.Asp9=
ENST00000539695.5:n.94G=
ENST00000541022.5:c.25G=	ENSP00000441230.1:p.Asp9=
ENST00000541564.5:c.25G=	ENSP00000443640.1:p.Asp9=
ENST00000541716.5:c.25G=	ENSP00000437729.1:p.Asp9=
ENST00000545434.5:c.25G=	ENSP00000445564.1:p.Asp9=
NM_002562.5:c.25G=	NP_002553.3:p.Asp9=
NR_033948.1:n.168G=
NR_033949.1:n.168G=
NR_033950.1:n.168G=
NR_033951.1:n.168G=
NR_033952.1:n.168G=
NR_033953.1:n.177G=
NR_033954.1:n.168G=
NR_033955.1:n.168G=
NR_033956.1:n.168G=
XM_011538418.1:c.25G=	XP_011536720.1:p.Asp9=
XM_011538419.1:c.-119G=	XP_011536721.1:n.-119G=
XM_011538419.3:c.-119G=	XP_011536721.1:n.-119G=
XM_017019364.2:c.-489G=	XP_016874853.1:n.-489G=
XM_017019365.2:c.-320G=	XP_016874854.1:n.-320G=
XM_017019366.2:c.-656G=	XP_016874855.1:n.-656G=
XM_017019367.2:c.-487G=	XP_016874856.1:n.-487G=
XR_001749352.2:n.187-6154C=
XR_001749354.2:n.187-6154C=
NM_002562.6:c.25G= MANE Select	NP_002553.3:p.Asp9=
NR_033948.2:n.120G=
NR_033949.2:n.120G=
NR_033950.2:n.120G=
NR_033951.2:n.120G=
NR_033952.2:n.120G=
NR_033953.2:n.120G=
NR_033954.2:n.120G=
NR_033955.2:n.120G=
NR_033956.2:n.120G=