Canonical Allele Identifier: CA2067768506
Gene: P2RX7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.121132986A= , CM000674.2:g.121132986A= GRCh38
NC_000012.11:g.121570789A= , CM000674.1:g.121570789A= GRCh37
NC_000012.10:g.120055172A= NCBI36
NG_011471.2:g.5112A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000328963.10:c.16A= MANE Select ENSP00000330696.6:p.Ser6=
ENST00000261826.10:c.16A= ENSP00000261826.6:p.Ser6=
ENST00000328963.9:c.16A= ENSP00000330696.6:p.Ser6=
ENST00000535250.5:c.16A= ENSP00000442572.2:p.Ser6=
ENST00000535600.2:c.16A= ENSP00000442470.1:p.Ser6=
ENST00000535928.5:c.16A= ENSP00000439961.1:p.Ser6=
ENST00000537312.5:c.16A= ENSP00000438586.1:p.Ser6=
ENST00000538011.5:c.16A= ENSP00000439247.1:p.Ser6=
ENST00000539606.5:c.16A= ENSP00000445325.1:p.Ser6=
ENST00000539695.5:n.85A=
ENST00000541022.5:c.16A= ENSP00000441230.1:p.Ser6=
ENST00000541564.5:c.16A= ENSP00000443640.1:p.Ser6=
ENST00000541716.5:c.16A= ENSP00000437729.1:p.Ser6=
ENST00000545434.5:c.16A= ENSP00000445564.1:p.Ser6=
NM_002562.5:c.16A= NP_002553.3:p.Ser6=
NR_033948.1:n.159A=
NR_033949.1:n.159A=
NR_033950.1:n.159A=
NR_033951.1:n.159A=
NR_033952.1:n.159A=
NR_033953.1:n.168A=
NR_033954.1:n.159A=
NR_033955.1:n.159A=
NR_033956.1:n.159A=
XM_011538418.1:c.16A= XP_011536720.1:p.Ser6=
XM_011538419.1:c.-128A= XP_011536721.1:n.-128A=
XM_011538419.3:c.-128A= XP_011536721.1:n.-128A=
XM_017019364.2:c.-498A= XP_016874853.1:n.-498A=
XM_017019365.2:c.-329A= XP_016874854.1:n.-329A=
XM_017019366.2:c.-665A= XP_016874855.1:n.-665A=
XM_017019367.2:c.-496A= XP_016874856.1:n.-496A=
XR_001749352.2:n.187-6145T=
XR_001749354.2:n.187-6145T=
NM_002562.6:c.16A= MANE Select NP_002553.3:p.Ser6=
NR_033948.2:n.111A=
NR_033949.2:n.111A=
NR_033950.2:n.111A=
NR_033951.2:n.111A=
NR_033952.2:n.111A=
NR_033953.2:n.111A=
NR_033954.2:n.111A=
NR_033955.2:n.111A=
NR_033956.2:n.111A=