Canonical Allele Identifier: CA2797733432
Gene: P2RX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.121222150del , CM000674.2:g.121222150del GRCh38
NC_000012.11:g.121659953del , CM000674.1:g.121659953del GRCh37
NC_000012.10:g.120144336del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000337233.9:c.411del MANE Select ENSP00000336607.4:p.Gly138AlafsTer13
ENST00000314442.7:n.4545del
ENST00000337233.8:c.411del ENSP00000336607.4:p.Gly138AlafsTer13
ENST00000359949.11:c.459del ENSP00000353032.7:p.Gly154AlafsTer13
ENST00000499638.6:n.447del
ENST00000538417.2:c.341del
ENST00000538701.5:c.135-6383del ENSP00000444033.1:n.135-6383del
ENST00000540930.5:n.447del
ENST00000541187.5:n.257del
ENST00000542067.5:c.411del ENSP00000438329.1:p.Gly138AlafsTer15
ENST00000543171.5:c.411del ENSP00000438131.2:p.Gly138AlafsTer13
ENST00000543318.5:c.411del ENSP00000444274.1:p.Gly138AlafsTer?
ENST00000543430.5:n.459del
ENST00000543984.5:c.*104del ENSP00000439386.1:n.*104del
NM_001256796.1:c.459del NP_001243725.1:p.Gly154AlafsTer13
NM_001261397.1:c.411del NP_001248326.1:p.Gly138AlafsTer15
NM_001261398.1:c.411del NP_001248327.1:p.Gly138AlafsTer13
NM_002560.2:c.411del NP_002551.2:p.Gly138AlafsTer13
NR_046372.1:n.715del
NR_046373.1:n.567del
XM_011538416.1:c.135-6383del XP_011536718.1:n.135-6383del
XM_011538417.1:c.459del XP_011536719.1:p.Gly154AlafsTer13
XR_944559.1:n.519del
XM_011538416.2:c.135-6383del XP_011536718.1:n.135-6383del
XR_001748726.2:n.465del
XR_001748727.1:n.528del
XR_001748728.1:n.528del
XR_001748729.2:n.465del
XR_944559.2:n.518del
NM_001256796.2:c.459del NP_001243725.1:p.Gly154AlafsTer13
NM_001261397.2:c.411del NP_001248326.1:p.Gly138AlafsTer15
NM_001261398.2:c.411del NP_001248327.1:p.Gly138AlafsTer13
NM_002560.3:c.411del MANE Select NP_002551.2:p.Gly138AlafsTer13
NR_046372.2:n.447del
NR_046373.2:n.299del