Canonical Allele Identifier: CA655086873

Gene: P2RX7

Linked Data

• COSMIC: COSN26561359

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121132917G>T , CM000674.2:g.121132917G>T	GRCh38
NC_000012.11:g.121570720G>T , CM000674.1:g.121570720G>T	GRCh37
NC_000012.10:g.120055103G>T	NCBI36
NG_011471.2:g.5043G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328963.10:c.-54G>T MANE Select	ENSP00000330696.6:n.-54G>T
ENST00000328963.9:c.-54G>T	ENSP00000330696.6:n.-54G>T
ENST00000535928.5:c.-54G>T	ENSP00000439961.1:n.-54G>T
ENST00000537312.5:c.-54G>T	ENSP00000438586.1:n.-54G>T
ENST00000539695.5:n.16G>T
NM_002562.5:c.-54G>T	NP_002553.3:n.-54G>T
NR_033948.1:n.90G>T
NR_033949.1:n.90G>T
NR_033950.1:n.90G>T
NR_033951.1:n.90G>T
NR_033952.1:n.90G>T
NR_033953.1:n.99G>T
NR_033954.1:n.90G>T
NR_033955.1:n.90G>T
NR_033956.1:n.90G>T
XM_011538418.1:c.-54G>T	XP_011536720.1:n.-54G>T
XM_011538419.1:c.-197G>T	XP_011536721.1:n.-197G>T
XM_011538419.3:c.-197G>T	XP_011536721.1:n.-197G>T
XM_017019364.2:c.-567G>T	XP_016874853.1:n.-567G>T
XM_017019366.2:c.-734G>T	XP_016874855.1:n.-734G>T
XM_017019367.2:c.-565G>T	XP_016874856.1:n.-565G>T
XR_001749352.2:n.187-6076C>A
XR_001749354.2:n.187-6076C>A
NM_002562.6:c.-54G>T MANE Select	NP_002553.3:n.-54G>T
NR_033948.2:n.42G>T
NR_033949.2:n.42G>T
NR_033950.2:n.42G>T
NR_033951.2:n.42G>T
NR_033952.2:n.42G>T
NR_033953.2:n.42G>T
NR_033954.2:n.42G>T
NR_033955.2:n.42G>T
NR_033956.2:n.42G>T