Canonical Allele Identifier: CA2067768908

Gene: P2RX7

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121133224_121133229delinsAGCTGG , CM000674.2:g.121133224_121133229delinsAGCTGG	GRCh38
NC_000012.11:g.121571027_121571032delinsAGCTGG , CM000674.1:g.121571027_121571032delinsAGCTGG	GRCh37
NC_000012.10:g.120055410_120055415delinsAGCTGG	NCBI36
NG_011471.2:g.5350_5355delinsAGCTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328963.10:c.125+129_125+134delinsAGCTGG MANE Select	ENSP00000330696.6:n.125+129_125+134delinsAGCTGG
ENST00000261826.10:c.125+129_125+134delinsAGCTGG	ENSP00000261826.6:n.125+129_125+134delinsAGCTGG
ENST00000328963.9:c.125+129_125+134delinsAGCTGG	ENSP00000330696.6:n.125+129_125+134delinsAGCTGG
ENST00000535250.5:c.125+129_125+134delinsAGCTGG	ENSP00000442572.2:n.125+129_125+134delinsAGCTGG
ENST00000535600.2:c.125+129_125+134delinsAGCTGG	ENSP00000442470.1:n.125+129_125+134delinsAGCTGG
ENST00000535928.5:c.125+129_125+134delinsAGCTGG	ENSP00000439961.1:n.125+129_125+134delinsAGCTGG
ENST00000537312.5:c.125+129_125+134delinsAGCTGG	ENSP00000438586.1:n.125+129_125+134delinsAGCTGG
ENST00000538011.5:c.125+129_125+134delinsAGCTGG	ENSP00000439247.1:n.125+129_125+134delinsAGCTGG
ENST00000539606.5:c.125+129_125+134delinsAGCTGG	ENSP00000445325.1:n.125+129_125+134delinsAGCTGG
ENST00000539695.5:n.194+129_194+134delinsAGCTGG
ENST00000541022.5:c.125+129_125+134delinsAGCTGG	ENSP00000441230.1:n.125+129_125+134delinsAGCTGG
ENST00000541564.5:c.125+129_125+134delinsAGCTGG	ENSP00000443640.1:n.125+129_125+134delinsAGCTGG
ENST00000541716.5:c.125+129_125+134delinsAGCTGG	ENSP00000437729.1:n.125+129_125+134delinsAGCTGG
ENST00000545434.5:c.125+129_125+134delinsAGCTGG	ENSP00000445564.1:n.125+129_125+134delinsAGCTGG
NM_002562.5:c.125+129_125+134delinsAGCTGG	NP_002553.3:n.125+129_125+134delinsAGCTGG
NR_033948.1:n.268+129_268+134delinsAGCTGG
NR_033949.1:n.268+129_268+134delinsAGCTGG
NR_033950.1:n.268+129_268+134delinsAGCTGG
NR_033951.1:n.268+129_268+134delinsAGCTGG
NR_033952.1:n.268+129_268+134delinsAGCTGG
NR_033953.1:n.277+129_277+134delinsAGCTGG
NR_033954.1:n.268+129_268+134delinsAGCTGG
NR_033955.1:n.268+129_268+134delinsAGCTGG
NR_033956.1:n.268+129_268+134delinsAGCTGG
XM_011538418.1:c.125+129_125+134delinsAGCTGG	XP_011536720.1:n.125+129_125+134delinsAGCTGG
XM_011538419.1:c.-19+129_-19+134delinsAGCTGG	XP_011536721.1:n.-19+129_-19+134delinsAGCTGG
XM_011538420.1:c.-437+129_-437+134delinsAGCTGG	XP_011536722.1:n.-437+129_-437+134delinsAGCTGG
XM_011538419.3:c.-19+129_-19+134delinsAGCTGG	XP_011536721.1:n.-19+129_-19+134delinsAGCTGG
XM_011538420.3:c.-437+129_-437+134delinsAGCTGG	XP_011536722.1:n.-437+129_-437+134delinsAGCTGG
XM_017019364.2:c.-389+129_-389+134delinsAGCTGG	XP_016874853.1:n.-389+129_-389+134delinsAGCTGG
XM_017019365.2:c.-220+129_-220+134delinsAGCTGG	XP_016874854.1:n.-220+129_-220+134delinsAGCTGG
XM_017019366.2:c.-556+129_-556+134delinsAGCTGG	XP_016874855.1:n.-556+129_-556+134delinsAGCTGG
XM_017019367.2:c.-387+129_-387+134delinsAGCTGG	XP_016874856.1:n.-387+129_-387+134delinsAGCTGG
XR_001749352.2:n.187-6388_187-6383delinsCCAGCT
XR_001749354.2:n.187-6388_187-6383delinsCCAGCT
NM_002562.6:c.125+129_125+134delinsAGCTGG MANE Select	NP_002553.3:n.125+129_125+134delinsAGCTGG
NR_033948.2:n.220+129_220+134delinsAGCTGG
NR_033949.2:n.220+129_220+134delinsAGCTGG
NR_033950.2:n.220+129_220+134delinsAGCTGG
NR_033951.2:n.220+129_220+134delinsAGCTGG
NR_033952.2:n.220+129_220+134delinsAGCTGG
NR_033953.2:n.220+129_220+134delinsAGCTGG
NR_033954.2:n.220+129_220+134delinsAGCTGG
NR_033955.2:n.220+129_220+134delinsAGCTGG
NR_033956.2:n.220+129_220+134delinsAGCTGG