Canonical Allele Identifier: CA2067768090

Gene: P2RX7

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121132901G= , CM000674.2:g.121132901G=	GRCh38
NC_000012.11:g.121570704G= , CM000674.1:g.121570704G=	GRCh37
NC_000012.10:g.120055087G=	NCBI36
NG_011471.2:g.5027G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328963.10:c.-70G= MANE Select	ENSP00000330696.6:n.-70G=
ENST00000328963.9:c.-70G=	ENSP00000330696.6:n.-70G=
ENST00000535928.5:c.-70G=	ENSP00000439961.1:n.-70G=
ENST00000537312.5:c.-70G=	ENSP00000438586.1:n.-70G=
NM_002562.5:c.-70G=	NP_002553.3:n.-70G=
NR_033948.1:n.74G=
NR_033949.1:n.74G=
NR_033950.1:n.74G=
NR_033951.1:n.74G=
NR_033952.1:n.74G=
NR_033953.1:n.83G=
NR_033954.1:n.74G=
NR_033955.1:n.74G=
NR_033956.1:n.74G=
XM_011538418.1:c.-70G=	XP_011536720.1:n.-70G=
XM_011538419.1:c.-213G=	XP_011536721.1:n.-213G=
XM_011538419.3:c.-213G=	XP_011536721.1:n.-213G=
XM_017019364.2:c.-583G=	XP_016874853.1:n.-583G=
XM_017019366.2:c.-750G=	XP_016874855.1:n.-750G=
XM_017019367.2:c.-581G=	XP_016874856.1:n.-581G=
XR_001749352.2:n.187-6060C=
XR_001749354.2:n.187-6060C=
NM_002562.6:c.-70G= MANE Select	NP_002553.3:n.-70G=
NR_033948.2:n.26G=
NR_033949.2:n.26G=
NR_033950.2:n.26G=
NR_033951.2:n.26G=
NR_033952.2:n.26G=
NR_033953.2:n.26G=
NR_033954.2:n.26G=
NR_033955.2:n.26G=
NR_033956.2:n.26G=