Canonical Allele Identifier: CA2621395961

Gene: P2RX7

Linked Data

• gnomAD v4: 12-121133044-A-ATT

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121133045_121133046dup , CM000674.2:g.121133045_121133046dup	GRCh38
NC_000012.11:g.121570848_121570849dup , CM000674.1:g.121570848_121570849dup	GRCh37
NC_000012.10:g.120055231_120055232dup	NCBI36
NG_011471.2:g.5171_5172dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328963.10:c.75_76dup MANE Select	ENSP00000330696.6:p.Tyr26PhefsTer11
ENST00000261826.10:c.75_76dup	ENSP00000261826.6:p.Tyr26PhefsTer11
ENST00000328963.9:c.75_76dup	ENSP00000330696.6:p.Tyr26PhefsTer11
ENST00000535250.5:c.75_76dup	ENSP00000442572.2:p.Tyr26PhefsTer11
ENST00000535600.2:c.75_76dup	ENSP00000442470.1:p.Tyr26PhefsTer11
ENST00000535928.5:c.75_76dup	ENSP00000439961.1:p.Tyr26PhefsTer11
ENST00000537312.5:c.75_76dup	ENSP00000438586.1:p.Tyr26PhefsTer11
ENST00000538011.5:c.75_76dup	ENSP00000439247.1:p.Tyr26PhefsTer11
ENST00000539606.5:c.75_76dup	ENSP00000445325.1:p.Tyr26PhefsTer11
ENST00000539695.5:n.144_145dup
ENST00000541022.5:c.75_76dup	ENSP00000441230.1:p.Tyr26PhefsTer11
ENST00000541564.5:c.75_76dup	ENSP00000443640.1:p.Tyr26PhefsTer11
ENST00000541716.5:c.75_76dup	ENSP00000437729.1:p.Tyr26PhefsTer11
ENST00000545434.5:c.75_76dup	ENSP00000445564.1:p.Tyr26PhefsTer11
NM_002562.5:c.75_76dup	NP_002553.3:p.Tyr26PhefsTer11
NR_033948.1:n.218_219dup
NR_033949.1:n.218_219dup
NR_033950.1:n.218_219dup
NR_033951.1:n.218_219dup
NR_033952.1:n.218_219dup
NR_033953.1:n.227_228dup
NR_033954.1:n.218_219dup
NR_033955.1:n.218_219dup
NR_033956.1:n.218_219dup
XM_011538418.1:c.75_76dup	XP_011536720.1:p.Tyr26PhefsTer11
XM_011538419.1:c.-69_-68dup	XP_011536721.1:n.-69_-68dup
XM_011538420.1:c.-487_-486dup	XP_011536722.1:n.-487_-486dup
XM_011538419.3:c.-69_-68dup	XP_011536721.1:n.-69_-68dup
XM_011538420.3:c.-487_-486dup	XP_011536722.1:n.-487_-486dup
XM_017019364.2:c.-439_-438dup	XP_016874853.1:n.-439_-438dup
XM_017019365.2:c.-270_-269dup	XP_016874854.1:n.-270_-269dup
XM_017019366.2:c.-606_-605dup	XP_016874855.1:n.-606_-605dup
XM_017019367.2:c.-437_-436dup	XP_016874856.1:n.-437_-436dup
XR_001749352.2:n.187-6205_187-6204dup
XR_001749354.2:n.187-6205_187-6204dup
NM_002562.6:c.75_76dup MANE Select	NP_002553.3:p.Tyr26PhefsTer11
NR_033948.2:n.170_171dup
NR_033949.2:n.170_171dup
NR_033950.2:n.170_171dup
NR_033951.2:n.170_171dup
NR_033952.2:n.170_171dup
NR_033953.2:n.170_171dup
NR_033954.2:n.170_171dup
NR_033955.2:n.170_171dup
NR_033956.2:n.170_171dup