Canonical Allele Identifier: CA2621395743

Gene: P2RX7

Linked Data

• gnomAD v4: 12-121132897-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121132902del , CM000674.2:g.121132902del	GRCh38
NC_000012.11:g.121570705del , CM000674.1:g.121570705del	GRCh37
NC_000012.10:g.120055088del	NCBI36
NG_011471.2:g.5028del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328963.10:c.-69del MANE Select	ENSP00000330696.6:n.-69del
ENST00000328963.9:c.-69del	ENSP00000330696.6:n.-69del
ENST00000535928.5:c.-69del	ENSP00000439961.1:n.-69del
ENST00000537312.5:c.-69del	ENSP00000438586.1:n.-69del
NM_002562.5:c.-69del	NP_002553.3:n.-69del
NR_033948.1:n.75del
NR_033949.1:n.75del
NR_033950.1:n.75del
NR_033951.1:n.75del
NR_033952.1:n.75del
NR_033953.1:n.84del
NR_033954.1:n.75del
NR_033955.1:n.75del
NR_033956.1:n.75del
XM_011538418.1:c.-69del	XP_011536720.1:n.-69del
XM_011538419.1:c.-212del	XP_011536721.1:n.-212del
XM_011538419.3:c.-212del	XP_011536721.1:n.-212del
XM_017019364.2:c.-582del	XP_016874853.1:n.-582del
XM_017019366.2:c.-749del	XP_016874855.1:n.-749del
XM_017019367.2:c.-580del	XP_016874856.1:n.-580del
XR_001749352.2:n.187-6057del
XR_001749354.2:n.187-6057del
NM_002562.6:c.-69del MANE Select	NP_002553.3:n.-69del
NR_033948.2:n.27del
NR_033949.2:n.27del
NR_033950.2:n.27del
NR_033951.2:n.27del
NR_033952.2:n.27del
NR_033953.2:n.27del
NR_033954.2:n.27del
NR_033955.2:n.27del
NR_033956.2:n.27del