Canonical Allele Identifier: CA2067768742

Gene: P2RX7

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121133118_121133128delinsCCAGATCTCTG , CM000674.2:g.121133118_121133128delinsCCAGATCTCTG	GRCh38
NC_000012.11:g.121570921_121570931delinsCCAGATCTCTG , CM000674.1:g.121570921_121570931delinsCCAGATCTCTG	GRCh37
NC_000012.10:g.120055304_120055314delinsCCAGATCTCTG	NCBI36
NG_011471.2:g.5244_5254delinsCCAGATCTCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328963.10:c.125+23_125+33delinsCCAGATCTCTG MANE Select	ENSP00000330696.6:n.125+23_125+33delinsCCAGATCTCTG
ENST00000261826.10:c.125+23_125+33delinsCCAGATCTCTG	ENSP00000261826.6:n.125+23_125+33delinsCCAGATCTCTG
ENST00000328963.9:c.125+23_125+33delinsCCAGATCTCTG	ENSP00000330696.6:n.125+23_125+33delinsCCAGATCTCTG
ENST00000535250.5:c.125+23_125+33delinsCCAGATCTCTG	ENSP00000442572.2:n.125+23_125+33delinsCCAGATCTCTG
ENST00000535600.2:c.125+23_125+33delinsCCAGATCTCTG	ENSP00000442470.1:n.125+23_125+33delinsCCAGATCTCTG
ENST00000535928.5:c.125+23_125+33delinsCCAGATCTCTG	ENSP00000439961.1:n.125+23_125+33delinsCCAGATCTCTG
ENST00000537312.5:c.125+23_125+33delinsCCAGATCTCTG	ENSP00000438586.1:n.125+23_125+33delinsCCAGATCTCTG
ENST00000538011.5:c.125+23_125+33delinsCCAGATCTCTG	ENSP00000439247.1:n.125+23_125+33delinsCCAGATCTCTG
ENST00000539606.5:c.125+23_125+33delinsCCAGATCTCTG	ENSP00000445325.1:n.125+23_125+33delinsCCAGATCTCTG
ENST00000539695.5:n.194+23_194+33delinsCCAGATCTCTG
ENST00000541022.5:c.125+23_125+33delinsCCAGATCTCTG	ENSP00000441230.1:n.125+23_125+33delinsCCAGATCTCTG
ENST00000541564.5:c.125+23_125+33delinsCCAGATCTCTG	ENSP00000443640.1:n.125+23_125+33delinsCCAGATCTCTG
ENST00000541716.5:c.125+23_125+33delinsCCAGATCTCTG	ENSP00000437729.1:n.125+23_125+33delinsCCAGATCTCTG
ENST00000545434.5:c.125+23_125+33delinsCCAGATCTCTG	ENSP00000445564.1:n.125+23_125+33delinsCCAGATCTCTG
NM_002562.5:c.125+23_125+33delinsCCAGATCTCTG	NP_002553.3:n.125+23_125+33delinsCCAGATCTCTG
NR_033948.1:n.268+23_268+33delinsCCAGATCTCTG
NR_033949.1:n.268+23_268+33delinsCCAGATCTCTG
NR_033950.1:n.268+23_268+33delinsCCAGATCTCTG
NR_033951.1:n.268+23_268+33delinsCCAGATCTCTG
NR_033952.1:n.268+23_268+33delinsCCAGATCTCTG
NR_033953.1:n.277+23_277+33delinsCCAGATCTCTG
NR_033954.1:n.268+23_268+33delinsCCAGATCTCTG
NR_033955.1:n.268+23_268+33delinsCCAGATCTCTG
NR_033956.1:n.268+23_268+33delinsCCAGATCTCTG
XM_011538418.1:c.125+23_125+33delinsCCAGATCTCTG	XP_011536720.1:n.125+23_125+33delinsCCAGATCTCTG
XM_011538419.1:c.-19+23_-19+33delinsCCAGATCTCTG	XP_011536721.1:n.-19+23_-19+33delinsCCAGATCTCTG
XM_011538420.1:c.-437+23_-437+33delinsCCAGATCTCTG	XP_011536722.1:n.-437+23_-437+33delinsCCAGATCTCTG
XM_011538419.3:c.-19+23_-19+33delinsCCAGATCTCTG	XP_011536721.1:n.-19+23_-19+33delinsCCAGATCTCTG
XM_011538420.3:c.-437+23_-437+33delinsCCAGATCTCTG	XP_011536722.1:n.-437+23_-437+33delinsCCAGATCTCTG
XM_017019364.2:c.-389+23_-389+33delinsCCAGATCTCTG	XP_016874853.1:n.-389+23_-389+33delinsCCAGATCTCTG
XM_017019365.2:c.-220+23_-220+33delinsCCAGATCTCTG	XP_016874854.1:n.-220+23_-220+33delinsCCAGATCTCTG
XM_017019366.2:c.-556+23_-556+33delinsCCAGATCTCTG	XP_016874855.1:n.-556+23_-556+33delinsCCAGATCTCTG
XM_017019367.2:c.-387+23_-387+33delinsCCAGATCTCTG	XP_016874856.1:n.-387+23_-387+33delinsCCAGATCTCTG
XR_001749352.2:n.187-6287_187-6277delinsCAGAGATCTGG
XR_001749354.2:n.187-6287_187-6277delinsCAGAGATCTGG
NM_002562.6:c.125+23_125+33delinsCCAGATCTCTG MANE Select	NP_002553.3:n.125+23_125+33delinsCCAGATCTCTG
NR_033948.2:n.220+23_220+33delinsCCAGATCTCTG
NR_033949.2:n.220+23_220+33delinsCCAGATCTCTG
NR_033950.2:n.220+23_220+33delinsCCAGATCTCTG
NR_033951.2:n.220+23_220+33delinsCCAGATCTCTG
NR_033952.2:n.220+23_220+33delinsCCAGATCTCTG
NR_033953.2:n.220+23_220+33delinsCCAGATCTCTG
NR_033954.2:n.220+23_220+33delinsCCAGATCTCTG
NR_033955.2:n.220+23_220+33delinsCCAGATCTCTG
NR_033956.2:n.220+23_220+33delinsCCAGATCTCTG