Canonical Allele Identifier: CA2067787224

Gene: P2RX7

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121177330T= , CM000674.2:g.121177330T=	GRCh38
NC_000012.11:g.121615133T= , CM000674.1:g.121615133T=	GRCh37
NC_000012.10:g.120099516T=	NCBI36
NG_011471.2:g.49456T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328963.10:c.1072T= MANE Select	ENSP00000330696.6:p.Tyr358=
ENST00000261826.10:c.*525T=	ENSP00000261826.6:n.*525T=
ENST00000328963.9:c.1072T=	ENSP00000330696.6:p.Tyr358=
ENST00000535250.5:c.1156T=	ENSP00000442572.2:n.1156T=
ENST00000535600.2:c.889T=	ENSP00000442470.1:n.889T=
ENST00000537312.5:c.*843T=	ENSP00000438586.1:n.*843T=
ENST00000538011.5:c.1211T=	ENSP00000439247.1:n.1211T=
ENST00000539606.5:c.1295T=	ENSP00000445325.1:n.1295T=
ENST00000539695.5:n.1241T=
ENST00000541022.5:c.862T=	ENSP00000441230.1:n.862T=
ENST00000541564.5:c.935T=	ENSP00000443640.1:n.935T=
ENST00000541716.5:c.1083T=	ENSP00000437729.1:n.1083T=
NM_002562.5:c.1072T=	NP_002553.3:p.Tyr358=
NR_033948.1:n.1438T=
NR_033949.1:n.1354T=
NR_033950.1:n.1315T=
NR_033951.1:n.1299T=
NR_033952.1:n.1226T=
NR_033953.1:n.1139T=
NR_033954.1:n.1118T=
NR_033955.1:n.1078T=
NR_033956.1:n.1005T=
XM_011538418.1:c.805T=	XP_011536720.1:p.Tyr269=
XM_011538419.1:c.760T=	XP_011536721.1:p.Tyr254=
XM_011538420.1:c.205T=	XP_011536722.1:p.Tyr69=
XR_945459.1:n.190-14913A=
XR_945460.1:n.299-14913A=
XM_011538419.3:c.760T=	XP_011536721.1:p.Tyr254=
XM_011538420.3:c.205T=	XP_011536722.1:p.Tyr69=
XM_017019364.2:c.712T=	XP_016874853.1:p.Tyr238=
XM_017019365.2:c.712T=	XP_016874854.1:p.Tyr238=
XM_017019366.2:c.319T=	XP_016874855.1:p.Tyr107=
XM_017019367.2:c.319T=	XP_016874856.1:p.Tyr107=
XR_001749352.2:n.186+26168A=
XR_001749353.2:n.304-14913A=
XR_001749354.2:n.186+26168A=
XR_945459.3:n.187-14913A=
XR_945460.3:n.299-14913A=
NM_002562.6:c.1072T= MANE Select	NP_002553.3:p.Tyr358=
NR_033948.2:n.1390T=
NR_033949.2:n.1306T=
NR_033950.2:n.1267T=
NR_033951.2:n.1251T=
NR_033952.2:n.1178T=
NR_033953.2:n.1082T=
NR_033954.2:n.1070T=
NR_033955.2:n.1030T=
NR_033956.2:n.957T=