Canonical Allele Identifier: CA2067768443

Gene: P2RX7

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121132959G= , CM000674.2:g.121132959G=	GRCh38
NC_000012.11:g.121570762G= , CM000674.1:g.121570762G=	GRCh37
NC_000012.10:g.120055145G=	NCBI36
NG_011471.2:g.5085G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328963.10:c.-12G= MANE Select	ENSP00000330696.6:n.-12G=
ENST00000261826.10:c.-12G=	ENSP00000261826.6:n.-12G=
ENST00000328963.9:c.-12G=	ENSP00000330696.6:n.-12G=
ENST00000535928.5:c.-12G=	ENSP00000439961.1:n.-12G=
ENST00000537312.5:c.-12G=	ENSP00000438586.1:n.-12G=
ENST00000539695.5:n.58G=
ENST00000545434.5:c.-12G=	ENSP00000445564.1:n.-12G=
NM_002562.5:c.-12G=	NP_002553.3:n.-12G=
NR_033948.1:n.132G=
NR_033949.1:n.132G=
NR_033950.1:n.132G=
NR_033951.1:n.132G=
NR_033952.1:n.132G=
NR_033953.1:n.141G=
NR_033954.1:n.132G=
NR_033955.1:n.132G=
NR_033956.1:n.132G=
XM_011538418.1:c.-12G=	XP_011536720.1:n.-12G=
XM_011538419.1:c.-155G=	XP_011536721.1:n.-155G=
XM_011538419.3:c.-155G=	XP_011536721.1:n.-155G=
XM_017019364.2:c.-525G=	XP_016874853.1:n.-525G=
XM_017019365.2:c.-356G=	XP_016874854.1:n.-356G=
XM_017019366.2:c.-692G=	XP_016874855.1:n.-692G=
XM_017019367.2:c.-523G=	XP_016874856.1:n.-523G=
XR_001749352.2:n.187-6118C=
XR_001749354.2:n.187-6118C=
NM_002562.6:c.-12G= MANE Select	NP_002553.3:n.-12G=
NR_033948.2:n.84G=
NR_033949.2:n.84G=
NR_033950.2:n.84G=
NR_033951.2:n.84G=
NR_033952.2:n.84G=
NR_033953.2:n.84G=
NR_033954.2:n.84G=
NR_033955.2:n.84G=
NR_033956.2:n.84G=