Canonical Allele Identifier: CA2067787291

Gene: P2RX7

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121177372A= , CM000674.2:g.121177372A=	GRCh38
NC_000012.11:g.121615175A= , CM000674.1:g.121615175A=	GRCh37
NC_000012.10:g.120099558A=	NCBI36
NG_011471.2:g.49498A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328963.10:c.1114A= MANE Select	ENSP00000330696.6:p.Lys372=
ENST00000261826.10:c.*567A=	ENSP00000261826.6:n.*567A=
ENST00000328963.9:c.1114A=	ENSP00000330696.6:p.Lys372=
ENST00000535250.5:c.1198A=	ENSP00000442572.2:n.1198A=
ENST00000535600.2:c.931A=	ENSP00000442470.1:n.931A=
ENST00000537312.5:c.*885A=	ENSP00000438586.1:n.*885A=
ENST00000538011.5:c.1253A=	ENSP00000439247.1:n.1253A=
ENST00000539606.5:c.1337A=	ENSP00000445325.1:n.1337A=
ENST00000539695.5:n.1283A=
ENST00000541022.5:c.904A=	ENSP00000441230.1:n.904A=
ENST00000541564.5:c.977A=	ENSP00000443640.1:n.977A=
ENST00000541716.5:c.1125A=	ENSP00000437729.1:n.1125A=
NM_002562.5:c.1114A=	NP_002553.3:p.Lys372=
NR_033948.1:n.1480A=
NR_033949.1:n.1396A=
NR_033950.1:n.1357A=
NR_033951.1:n.1341A=
NR_033952.1:n.1268A=
NR_033953.1:n.1181A=
NR_033954.1:n.1160A=
NR_033955.1:n.1120A=
NR_033956.1:n.1047A=
XM_011538418.1:c.847A=	XP_011536720.1:p.Lys283=
XM_011538419.1:c.802A=	XP_011536721.1:p.Lys268=
XM_011538420.1:c.247A=	XP_011536722.1:p.Lys83=
XR_945459.1:n.190-14955T=
XR_945460.1:n.299-14955T=
XM_011538419.3:c.802A=	XP_011536721.1:p.Lys268=
XM_011538420.3:c.247A=	XP_011536722.1:p.Lys83=
XM_017019364.2:c.754A=	XP_016874853.1:p.Lys252=
XM_017019365.2:c.754A=	XP_016874854.1:p.Lys252=
XM_017019366.2:c.361A=	XP_016874855.1:p.Lys121=
XM_017019367.2:c.361A=	XP_016874856.1:p.Lys121=
XR_001749352.2:n.186+26126T=
XR_001749353.2:n.304-14955T=
XR_001749354.2:n.186+26126T=
XR_945459.3:n.187-14955T=
XR_945460.3:n.299-14955T=
NM_002562.6:c.1114A= MANE Select	NP_002553.3:p.Lys372=
NR_033948.2:n.1432A=
NR_033949.2:n.1348A=
NR_033950.2:n.1309A=
NR_033951.2:n.1293A=
NR_033952.2:n.1220A=
NR_033953.2:n.1124A=
NR_033954.2:n.1112A=
NR_033955.2:n.1072A=
NR_033956.2:n.999A=