Canonical Allele Identifier: CA386948406
Gene: P2RX4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.121222120A>C , CM000674.2:g.121222120A>C GRCh38
NC_000012.11:g.121659923A>C , CM000674.1:g.121659923A>C GRCh37
NC_000012.10:g.120144306A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000337233.9:c.381A>C MANE Select ENSP00000336607.4:p.Lys127Asn
ENST00000314442.7:n.4515A>C
ENST00000337233.8:c.381A>C ENSP00000336607.4:p.Lys127Asn
ENST00000359949.11:c.429A>C ENSP00000353032.7:p.Lys143Asn
ENST00000499638.6:n.417A>C
ENST00000538417.2:c.311A>C
ENST00000538701.5:c.135-6413A>C ENSP00000444033.1:n.135-6413A>C
ENST00000540930.5:n.417A>C
ENST00000541187.5:n.227A>C
ENST00000542067.5:c.381A>C ENSP00000438329.1:p.Lys127Asn
ENST00000543171.5:c.381A>C ENSP00000438131.2:p.Lys127Asn
ENST00000543318.5:c.381A>C ENSP00000444274.1:p.Lys127Asn
ENST00000543430.5:n.429A>C
ENST00000543984.5:c.*74A>C ENSP00000439386.1:n.*74A>C
NM_001256796.1:c.429A>C NP_001243725.1:p.Lys143Asn
NM_001261397.1:c.381A>C NP_001248326.1:p.Lys127Asn
NM_001261398.1:c.381A>C NP_001248327.1:p.Lys127Asn
NM_002560.2:c.381A>C NP_002551.2:p.Lys127Asn
NR_046372.1:n.685A>C
NR_046373.1:n.537A>C
XM_011538416.1:c.135-6413A>C XP_011536718.1:n.135-6413A>C
XM_011538417.1:c.429A>C XP_011536719.1:p.Lys143Asn
XR_944559.1:n.489A>C
XM_011538416.2:c.135-6413A>C XP_011536718.1:n.135-6413A>C
XR_001748726.2:n.435A>C
XR_001748727.1:n.498A>C
XR_001748728.1:n.498A>C
XR_001748729.2:n.435A>C
XR_944559.2:n.488A>C
NM_001256796.2:c.429A>C NP_001243725.1:p.Lys143Asn
NM_001261397.2:c.381A>C NP_001248326.1:p.Lys127Asn
NM_001261398.2:c.381A>C NP_001248327.1:p.Lys127Asn
NM_002560.3:c.381A>C MANE Select NP_002551.2:p.Lys127Asn
NR_046372.2:n.417A>C
NR_046373.2:n.269A>C