Canonical Allele Identifier: CA2067769020

Gene: P2RX7

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121133303_121133304delinsCG , CM000674.2:g.121133303_121133304delinsCG	GRCh38
NC_000012.11:g.121571106_121571107delinsCG , CM000674.1:g.121571106_121571107delinsCG	GRCh37
NC_000012.10:g.120055489_120055490delinsCG	NCBI36
NG_011471.2:g.5429_5430delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328963.10:c.125+208_125+209delinsCG MANE Select	ENSP00000330696.6:n.125+208_125+209delinsCG
ENST00000261826.10:c.125+208_125+209delinsCG	ENSP00000261826.6:n.125+208_125+209delinsCG
ENST00000328963.9:c.125+208_125+209delinsCG	ENSP00000330696.6:n.125+208_125+209delinsCG
ENST00000535250.5:c.125+208_125+209delinsCG	ENSP00000442572.2:n.125+208_125+209delinsCG
ENST00000535600.2:c.125+208_125+209delinsCG	ENSP00000442470.1:n.125+208_125+209delinsCG
ENST00000535928.5:c.125+208_125+209delinsCG	ENSP00000439961.1:n.125+208_125+209delinsCG
ENST00000537312.5:c.125+208_125+209delinsCG	ENSP00000438586.1:n.125+208_125+209delinsCG
ENST00000538011.5:c.125+208_125+209delinsCG	ENSP00000439247.1:n.125+208_125+209delinsCG
ENST00000539606.5:c.125+208_125+209delinsCG	ENSP00000445325.1:n.125+208_125+209delinsCG
ENST00000539695.5:n.194+208_194+209delinsCG
ENST00000541022.5:c.125+208_125+209delinsCG	ENSP00000441230.1:n.125+208_125+209delinsCG
ENST00000541564.5:c.125+208_125+209delinsCG	ENSP00000443640.1:n.125+208_125+209delinsCG
ENST00000541716.5:c.125+208_125+209delinsCG	ENSP00000437729.1:n.125+208_125+209delinsCG
ENST00000545434.5:c.125+208_125+209delinsCG	ENSP00000445564.1:n.125+208_125+209delinsCG
NM_002562.5:c.125+208_125+209delinsCG	NP_002553.3:n.125+208_125+209delinsCG
NR_033948.1:n.268+208_268+209delinsCG
NR_033949.1:n.268+208_268+209delinsCG
NR_033950.1:n.268+208_268+209delinsCG
NR_033951.1:n.268+208_268+209delinsCG
NR_033952.1:n.268+208_268+209delinsCG
NR_033953.1:n.277+208_277+209delinsCG
NR_033954.1:n.268+208_268+209delinsCG
NR_033955.1:n.268+208_268+209delinsCG
NR_033956.1:n.268+208_268+209delinsCG
XM_011538418.1:c.125+208_125+209delinsCG	XP_011536720.1:n.125+208_125+209delinsCG
XM_011538419.1:c.-19+208_-19+209delinsCG	XP_011536721.1:n.-19+208_-19+209delinsCG
XM_011538420.1:c.-437+208_-437+209delinsCG	XP_011536722.1:n.-437+208_-437+209delinsCG
XM_011538419.3:c.-19+208_-19+209delinsCG	XP_011536721.1:n.-19+208_-19+209delinsCG
XM_011538420.3:c.-437+208_-437+209delinsCG	XP_011536722.1:n.-437+208_-437+209delinsCG
XM_017019364.2:c.-389+208_-389+209delinsCG	XP_016874853.1:n.-389+208_-389+209delinsCG
XM_017019365.2:c.-220+208_-220+209delinsCG	XP_016874854.1:n.-220+208_-220+209delinsCG
XM_017019366.2:c.-556+208_-556+209delinsCG	XP_016874855.1:n.-556+208_-556+209delinsCG
XM_017019367.2:c.-387+208_-387+209delinsCG	XP_016874856.1:n.-387+208_-387+209delinsCG
XR_001749352.2:n.187-6463_187-6462delinsCG
XR_001749354.2:n.187-6463_187-6462delinsCG
NM_002562.6:c.125+208_125+209delinsCG MANE Select	NP_002553.3:n.125+208_125+209delinsCG
NR_033948.2:n.220+208_220+209delinsCG
NR_033949.2:n.220+208_220+209delinsCG
NR_033950.2:n.220+208_220+209delinsCG
NR_033951.2:n.220+208_220+209delinsCG
NR_033952.2:n.220+208_220+209delinsCG
NR_033953.2:n.220+208_220+209delinsCG
NR_033954.2:n.220+208_220+209delinsCG
NR_033955.2:n.220+208_220+209delinsCG
NR_033956.2:n.220+208_220+209delinsCG