Canonical Allele Identifier: CA6833932
Gene: P2RX4 HGNC NCBI

Linked Data

dbSNP Id: rs765866317

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.121222142G>A , CM000674.2:g.121222142G>A GRCh38
NC_000012.11:g.121659945G>A , CM000674.1:g.121659945G>A GRCh37
NC_000012.10:g.120144328G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000337233.9:c.403G>A MANE Select ENSP00000336607.4:p.Gly135Ser
ENST00000314442.7:n.4537G>A
ENST00000337233.8:c.403G>A ENSP00000336607.4:p.Gly135Ser
ENST00000359949.11:c.451G>A ENSP00000353032.7:p.Gly151Ser
ENST00000499638.6:n.439G>A
ENST00000538417.2:c.333G>A
ENST00000538701.5:c.135-6391G>A ENSP00000444033.1:n.135-6391G>A
ENST00000540930.5:n.439G>A
ENST00000541187.5:n.249G>A
ENST00000542067.5:c.403G>A ENSP00000438329.1:p.Gly135Ser
ENST00000543171.5:c.403G>A ENSP00000438131.2:p.Gly135Ser
ENST00000543318.5:c.403G>A ENSP00000444274.1:p.Gly135Ser
ENST00000543430.5:n.451G>A
ENST00000543984.5:c.*96G>A ENSP00000439386.1:n.*96G>A
NM_001256796.1:c.451G>A NP_001243725.1:p.Gly151Ser
NM_001261397.1:c.403G>A NP_001248326.1:p.Gly135Ser
NM_001261398.1:c.403G>A NP_001248327.1:p.Gly135Ser
NM_002560.2:c.403G>A NP_002551.2:p.Gly135Ser
NR_046372.1:n.707G>A
NR_046373.1:n.559G>A
XM_011538416.1:c.135-6391G>A XP_011536718.1:n.135-6391G>A
XM_011538417.1:c.451G>A XP_011536719.1:p.Gly151Ser
XR_944559.1:n.511G>A
XM_011538416.2:c.135-6391G>A XP_011536718.1:n.135-6391G>A
XR_001748726.2:n.457G>A
XR_001748727.1:n.520G>A
XR_001748728.1:n.520G>A
XR_001748729.2:n.457G>A
XR_944559.2:n.510G>A
NM_001256796.2:c.451G>A NP_001243725.1:p.Gly151Ser
NM_001261397.2:c.403G>A NP_001248326.1:p.Gly135Ser
NM_001261398.2:c.403G>A NP_001248327.1:p.Gly135Ser
NM_002560.3:c.403G>A MANE Select NP_002551.2:p.Gly135Ser
NR_046372.2:n.439G>A
NR_046373.2:n.291G>A