Canonical Allele Identifier: CA386947700

Gene: P2RX4

Linked Data

• MyVariant Identifiers: chr12:g.121659723A>T (hg19) ; chr12:g.121221920A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121221920A>T , CM000674.2:g.121221920A>T	GRCh38
NC_000012.11:g.121659723A>T , CM000674.1:g.121659723A>T	GRCh37
NC_000012.10:g.120144106A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337233.9:c.290A>T MANE Select	ENSP00000336607.4:p.Asn97Ile
ENST00000314442.7:n.4424A>T
ENST00000337233.8:c.290A>T	ENSP00000336607.4:p.Asn97Ile
ENST00000359949.11:c.338A>T	ENSP00000353032.7:p.Asn113Ile
ENST00000499638.6:n.326A>T
ENST00000538417.2:c.220A>T
ENST00000538701.5:c.135-6613A>T	ENSP00000444033.1:n.135-6613A>T
ENST00000540930.5:n.326A>T
ENST00000541187.5:n.136A>T
ENST00000542067.5:c.290A>T	ENSP00000438329.1:p.Asn97Ile
ENST00000543171.5:c.290A>T	ENSP00000438131.2:p.Asn97Ile
ENST00000543318.5:c.290A>T	ENSP00000444274.1:p.Asn97Ile
ENST00000543430.5:n.338A>T
ENST00000543984.5:c.142A>T	ENSP00000439386.1:p.Thr48Ser
NM_001256796.1:c.338A>T	NP_001243725.1:p.Asn113Ile
NM_001261397.1:c.290A>T	NP_001248326.1:p.Asn97Ile
NM_001261398.1:c.290A>T	NP_001248327.1:p.Asn97Ile
NM_002560.2:c.290A>T	NP_002551.2:p.Asn97Ile
NR_046372.1:n.594A>T
NR_046373.1:n.446A>T
XM_011538416.1:c.135-6613A>T	XP_011536718.1:n.135-6613A>T
XM_011538417.1:c.338A>T	XP_011536719.1:p.Asn113Ile
XR_944559.1:n.398A>T
XM_011538416.2:c.135-6613A>T	XP_011536718.1:n.135-6613A>T
XR_001748726.2:n.344A>T
XR_001748727.1:n.407A>T
XR_001748728.1:n.407A>T
XR_001748729.2:n.344A>T
XR_944559.2:n.397A>T
NM_001256796.2:c.338A>T	NP_001243725.1:p.Asn113Ile
NM_001261397.2:c.290A>T	NP_001248326.1:p.Asn97Ile
NM_001261398.2:c.290A>T	NP_001248327.1:p.Asn97Ile
NM_002560.3:c.290A>T MANE Select	NP_002551.2:p.Asn97Ile
NR_046372.2:n.326A>T
NR_046373.2:n.178A>T