Canonical Allele Identifier: CA2840768213
Gene: P2RX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.121222158dup , CM000674.2:g.121222158dup GRCh38
NC_000012.11:g.121659961dup , CM000674.1:g.121659961dup GRCh37
NC_000012.10:g.120144344dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000337233.9:c.419dup MANE Select ENSP00000336607.4:p.His140GlnfsTer21
ENST00000314442.7:n.4553dup
ENST00000337233.8:c.419dup ENSP00000336607.4:p.His140GlnfsTer21
ENST00000359949.11:c.467dup ENSP00000353032.7:p.His156GlnfsTer21
ENST00000499638.6:n.455dup
ENST00000538417.2:c.349dup
ENST00000538701.5:c.135-6375dup ENSP00000444033.1:n.135-6375dup
ENST00000540930.5:n.455dup
ENST00000541187.5:n.265dup
ENST00000542067.5:c.419dup ENSP00000438329.1:p.His140GlnfsTer24
ENST00000543171.5:c.419dup ENSP00000438131.2:p.His140GlnfsTer21
ENST00000543318.5:c.419dup ENSP00000444274.1:p.His140GlnfsTer?
ENST00000543430.5:n.467dup
ENST00000543984.5:c.*112dup ENSP00000439386.1:n.*112dup
NM_001256796.1:c.467dup NP_001243725.1:p.His156GlnfsTer21
NM_001261397.1:c.419dup NP_001248326.1:p.His140GlnfsTer24
NM_001261398.1:c.419dup NP_001248327.1:p.His140GlnfsTer21
NM_002560.2:c.419dup NP_002551.2:p.His140GlnfsTer21
NR_046372.1:n.723dup
NR_046373.1:n.575dup
XM_011538416.1:c.135-6375dup XP_011536718.1:n.135-6375dup
XM_011538417.1:c.467dup XP_011536719.1:p.His156GlnfsTer21
XR_944559.1:n.527dup
XM_011538416.2:c.135-6375dup XP_011536718.1:n.135-6375dup
XR_001748726.2:n.473dup
XR_001748727.1:n.536dup
XR_001748728.1:n.536dup
XR_001748729.2:n.473dup
XR_944559.2:n.526dup
NM_001256796.2:c.467dup NP_001243725.1:p.His156GlnfsTer21
NM_001261397.2:c.419dup NP_001248326.1:p.His140GlnfsTer24
NM_001261398.2:c.419dup NP_001248327.1:p.His140GlnfsTer21
NM_002560.3:c.419dup MANE Select NP_002551.2:p.His140GlnfsTer21
NR_046372.2:n.455dup
NR_046373.2:n.307dup