Canonical Allele Identifier: CA2067787393

Gene: P2RX7

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121177426T= , CM000674.2:g.121177426T=	GRCh38
NC_000012.11:g.121615229T= , CM000674.1:g.121615229T=	GRCh37
NC_000012.10:g.120099612T=	NCBI36
NG_011471.2:g.49552T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328963.10:c.1168T= MANE Select	ENSP00000330696.6:p.Ser390=
ENST00000261826.10:c.*621T=	ENSP00000261826.6:n.*621T=
ENST00000328963.9:c.1168T=	ENSP00000330696.6:p.Ser390=
ENST00000535250.5:c.1252T=	ENSP00000442572.2:n.1252T=
ENST00000535600.2:c.985T=	ENSP00000442470.1:n.985T=
ENST00000537312.5:c.*939T=	ENSP00000438586.1:n.*939T=
ENST00000538011.5:c.1307T=	ENSP00000439247.1:n.1307T=
ENST00000539606.5:c.1391T=	ENSP00000445325.1:n.1391T=
ENST00000539695.5:n.1337T=
ENST00000541022.5:c.958T=	ENSP00000441230.1:n.958T=
ENST00000541564.5:c.1031T=	ENSP00000443640.1:n.1031T=
ENST00000541716.5:c.1179T=	ENSP00000437729.1:n.1179T=
NM_002562.5:c.1168T=	NP_002553.3:p.Ser390=
NR_033948.1:n.1534T=
NR_033949.1:n.1450T=
NR_033950.1:n.1411T=
NR_033951.1:n.1395T=
NR_033952.1:n.1322T=
NR_033953.1:n.1235T=
NR_033954.1:n.1214T=
NR_033955.1:n.1174T=
NR_033956.1:n.1101T=
XM_011538418.1:c.901T=	XP_011536720.1:p.Ser301=
XM_011538419.1:c.856T=	XP_011536721.1:p.Ser286=
XM_011538420.1:c.301T=	XP_011536722.1:p.Ser101=
XR_945459.1:n.190-15009A=
XR_945460.1:n.299-15009A=
XM_011538419.3:c.856T=	XP_011536721.1:p.Ser286=
XM_011538420.3:c.301T=	XP_011536722.1:p.Ser101=
XM_017019364.2:c.808T=	XP_016874853.1:p.Ser270=
XM_017019365.2:c.808T=	XP_016874854.1:p.Ser270=
XM_017019366.2:c.415T=	XP_016874855.1:p.Ser139=
XM_017019367.2:c.415T=	XP_016874856.1:p.Ser139=
XR_001749352.2:n.186+26072A=
XR_001749353.2:n.304-15009A=
XR_001749354.2:n.186+26072A=
XR_945459.3:n.187-15009A=
XR_945460.3:n.299-15009A=
NM_002562.6:c.1168T= MANE Select	NP_002553.3:p.Ser390=
NR_033948.2:n.1486T=
NR_033949.2:n.1402T=
NR_033950.2:n.1363T=
NR_033951.2:n.1347T=
NR_033952.2:n.1274T=
NR_033953.2:n.1178T=
NR_033954.2:n.1166T=
NR_033955.2:n.1126T=
NR_033956.2:n.1053T=