Canonical Allele Identifier: CA2067768362
Gene: P2RX7 HGNC NCBI

Linked Data

dbSNP Id: rs1872722558

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.121132933_121132936dup , CM000674.2:g.121132933_121132936dup GRCh38
NC_000012.11:g.121570736_121570739dup , CM000674.1:g.121570736_121570739dup GRCh37
NC_000012.10:g.120055119_120055122dup NCBI36
NG_011471.2:g.5059_5062dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000328963.10:c.-38_-35dup MANE Select ENSP00000330696.6:n.-38_-35dup
ENST00000261826.10:c.-38_-35dup ENSP00000261826.6:n.-38_-35dup
ENST00000328963.9:c.-38_-35dup ENSP00000330696.6:n.-38_-35dup
ENST00000535928.5:c.-38_-35dup ENSP00000439961.1:n.-38_-35dup
ENST00000537312.5:c.-38_-35dup ENSP00000438586.1:n.-38_-35dup
ENST00000539695.5:n.32_35dup
ENST00000545434.5:c.-38_-35dup ENSP00000445564.1:n.-38_-35dup
NM_002562.5:c.-38_-35dup NP_002553.3:n.-38_-35dup
NR_033948.1:n.106_109dup
NR_033949.1:n.106_109dup
NR_033950.1:n.106_109dup
NR_033951.1:n.106_109dup
NR_033952.1:n.106_109dup
NR_033953.1:n.115_118dup
NR_033954.1:n.106_109dup
NR_033955.1:n.106_109dup
NR_033956.1:n.106_109dup
XM_011538418.1:c.-38_-35dup XP_011536720.1:n.-38_-35dup
XM_011538419.1:c.-181_-178dup XP_011536721.1:n.-181_-178dup
XM_011538419.3:c.-181_-178dup XP_011536721.1:n.-181_-178dup
XM_017019364.2:c.-551_-548dup XP_016874853.1:n.-551_-548dup
XM_017019365.2:c.-382_-379dup XP_016874854.1:n.-382_-379dup
XM_017019366.2:c.-718_-715dup XP_016874855.1:n.-718_-715dup
XM_017019367.2:c.-549_-546dup XP_016874856.1:n.-549_-546dup
XR_001749352.2:n.187-6095_187-6092dup
XR_001749354.2:n.187-6095_187-6092dup
NM_002562.6:c.-38_-35dup MANE Select NP_002553.3:n.-38_-35dup
NR_033948.2:n.58_61dup
NR_033949.2:n.58_61dup
NR_033950.2:n.58_61dup
NR_033951.2:n.58_61dup
NR_033952.2:n.58_61dup
NR_033953.2:n.58_61dup
NR_033954.2:n.58_61dup
NR_033955.2:n.58_61dup
NR_033956.2:n.58_61dup