Canonical Allele Identifier: CA6891573
Gene: P2RX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.132620348del , CM000674.2:g.132620348del GRCh38
NC_000012.11:g.133196934del , CM000674.1:g.133196934del GRCh37
NC_000012.10:g.131707007del NCBI36
NG_033909.1:g.6569del

Transcript Alleles

HGVS Amino-acid Change
NM_170682.4:c.635+1del MANE Select NP_733782.1:n.635+1del
ENST00000643471.2:c.635+1del MANE Select ENSP00000494644.1:n.635+1del
NM_001282164.1:c.528+1del NP_001269093.1:n.528+1del
NM_001282164.2:c.528+1del NP_001269093.1:n.528+1del
NM_001282165.1:c.635+1del NP_001269094.1:n.635+1del
NM_001282165.2:c.635+1del NP_001269094.1:n.635+1del
NM_012226.4:c.419+1del NP_036358.2:n.419+1del
NM_012226.5:c.419+1del NP_036358.2:n.419+1del
NM_016318.3:c.563+1del NP_057402.1:n.563+1del
NM_016318.4:c.563+1del NP_057402.1:n.563+1del
NM_170682.3:c.635+1del NP_733782.1:n.635+1del
NM_170683.3:c.635+1del NP_733783.1:n.635+1del
NM_170683.4:c.635+1del NP_733783.1:n.635+1del
NM_174872.2:c.359+1del NP_777361.1:n.359+1del
NM_174872.3:c.359+1del NP_777361.1:n.359+1del
NM_174873.2:c.635+1del NP_777362.1:n.635+1del
NM_174873.3:c.635+1del NP_777362.1:n.635+1del
ENST00000343948.8:c.635+1del ENSP00000343339.4:n.635+1del
ENST00000348800.9:c.635+1del ENSP00000345095.5:n.635+1del
ENST00000350048.9:c.563+1del ENSP00000343904.5:n.563+1del
ENST00000351222.8:c.359+1del ENSP00000344502.4:n.359+1del
ENST00000352418.8:c.419+1del ENSP00000341419.4:n.419+1del
ENST00000389110.7:c.635+1del ENSP00000373762.3:n.635+1del
ENST00000449132.6:c.528+1del ENSP00000405531.2:n.528+1del
ENST00000542301.2:c.635+1del ENSP00000444477.2:n.635+1del
XM_005266154.2:c.635+1del XP_005266211.1:n.635+1del
XM_005266154.4:c.635+1del XP_005266211.1:n.635+1del
XM_005266155.3:c.635+1del XP_005266212.1:n.635+1del
XM_005266155.5:c.635+1del XP_005266212.1:n.635+1del
XM_005266156.3:c.635+1del XP_005266213.1:n.635+1del
XM_005266156.5:c.635+1del XP_005266213.1:n.635+1del
XM_011534786.1:c.563+1del XP_011533088.1:n.563+1del
XM_011534786.3:c.563+1del XP_011533088.1:n.563+1del
XM_017019035.2:c.635+1del XP_016874524.1:n.635+1del