Canonical Allele Identifier: CA2067768343
Gene: P2RX7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.121132924_121132927delinsAGAG , CM000674.2:g.121132924_121132927delinsAGAG GRCh38
NC_000012.11:g.121570727_121570730delinsAGAG , CM000674.1:g.121570727_121570730delinsAGAG GRCh37
NC_000012.10:g.120055110_120055113delinsAGAG NCBI36
NG_011471.2:g.5050_5053delinsAGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000328963.10:c.-47_-44delinsAGAG MANE Select ENSP00000330696.6:n.-47_-44delinsAGAG
ENST00000328963.9:c.-47_-44delinsAGAG ENSP00000330696.6:n.-47_-44delinsAGAG
ENST00000535928.5:c.-47_-44delinsAGAG ENSP00000439961.1:n.-47_-44delinsAGAG
ENST00000537312.5:c.-47_-44delinsAGAG ENSP00000438586.1:n.-47_-44delinsAGAG
ENST00000539695.5:n.23_26delinsAGAG
NM_002562.5:c.-47_-44delinsAGAG NP_002553.3:n.-47_-44delinsAGAG
NR_033948.1:n.97_100delinsAGAG
NR_033949.1:n.97_100delinsAGAG
NR_033950.1:n.97_100delinsAGAG
NR_033951.1:n.97_100delinsAGAG
NR_033952.1:n.97_100delinsAGAG
NR_033953.1:n.106_109delinsAGAG
NR_033954.1:n.97_100delinsAGAG
NR_033955.1:n.97_100delinsAGAG
NR_033956.1:n.97_100delinsAGAG
XM_011538418.1:c.-47_-44delinsAGAG XP_011536720.1:n.-47_-44delinsAGAG
XM_011538419.1:c.-190_-187delinsAGAG XP_011536721.1:n.-190_-187delinsAGAG
XM_011538419.3:c.-190_-187delinsAGAG XP_011536721.1:n.-190_-187delinsAGAG
XM_017019364.2:c.-560_-557delinsAGAG XP_016874853.1:n.-560_-557delinsAGAG
XM_017019366.2:c.-727_-724delinsAGAG XP_016874855.1:n.-727_-724delinsAGAG
XM_017019367.2:c.-558_-555delinsAGAG XP_016874856.1:n.-558_-555delinsAGAG
XR_001749352.2:n.187-6086_187-6083delinsCTCT
XR_001749354.2:n.187-6086_187-6083delinsCTCT
NM_002562.6:c.-47_-44delinsAGAG MANE Select NP_002553.3:n.-47_-44delinsAGAG
NR_033948.2:n.49_52delinsAGAG
NR_033949.2:n.49_52delinsAGAG
NR_033950.2:n.49_52delinsAGAG
NR_033951.2:n.49_52delinsAGAG
NR_033952.2:n.49_52delinsAGAG
NR_033953.2:n.49_52delinsAGAG
NR_033954.2:n.49_52delinsAGAG
NR_033955.2:n.49_52delinsAGAG
NR_033956.2:n.49_52delinsAGAG