Canonical Allele Identifier: CA2621395750

Gene: P2RX7

Linked Data

• gnomAD v4: 12-121132910-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121132912del , CM000674.2:g.121132912del	GRCh38
NC_000012.11:g.121570715del , CM000674.1:g.121570715del	GRCh37
NC_000012.10:g.120055098del	NCBI36
NG_011471.2:g.5038del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328963.10:c.-59del MANE Select	ENSP00000330696.6:n.-59del
ENST00000328963.9:c.-59del	ENSP00000330696.6:n.-59del
ENST00000535928.5:c.-59del	ENSP00000439961.1:n.-59del
ENST00000537312.5:c.-59del	ENSP00000438586.1:n.-59del
ENST00000539695.5:n.11del
NM_002562.5:c.-59del	NP_002553.3:n.-59del
NR_033948.1:n.85del
NR_033949.1:n.85del
NR_033950.1:n.85del
NR_033951.1:n.85del
NR_033952.1:n.85del
NR_033953.1:n.94del
NR_033954.1:n.85del
NR_033955.1:n.85del
NR_033956.1:n.85del
XM_011538418.1:c.-59del	XP_011536720.1:n.-59del
XM_011538419.1:c.-202del	XP_011536721.1:n.-202del
XM_011538419.3:c.-202del	XP_011536721.1:n.-202del
XM_017019364.2:c.-572del	XP_016874853.1:n.-572del
XM_017019366.2:c.-739del	XP_016874855.1:n.-739del
XM_017019367.2:c.-570del	XP_016874856.1:n.-570del
XR_001749352.2:n.187-6070del
XR_001749354.2:n.187-6070del
NM_002562.6:c.-59del MANE Select	NP_002553.3:n.-59del
NR_033948.2:n.37del
NR_033949.2:n.37del
NR_033950.2:n.37del
NR_033951.2:n.37del
NR_033952.2:n.37del
NR_033953.2:n.37del
NR_033954.2:n.37del
NR_033955.2:n.37del
NR_033956.2:n.37del