Canonical Allele Identifier: CA2067739795

Gene: P2RX4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121222098C= , CM000674.2:g.121222098C=	GRCh38
NC_000012.11:g.121659901C= , CM000674.1:g.121659901C=	GRCh37
NC_000012.10:g.120144284C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337233.9:c.359C= MANE Select	ENSP00000336607.4:p.Pro120=
ENST00000314442.7:n.4493C=
ENST00000337233.8:c.359C=	ENSP00000336607.4:p.Pro120=
ENST00000359949.11:c.407C=	ENSP00000353032.7:p.Pro136=
ENST00000499638.6:n.395C=
ENST00000538417.2:c.289C=
ENST00000538701.5:c.135-6435C=	ENSP00000444033.1:n.135-6435C=
ENST00000540930.5:n.395C=
ENST00000541187.5:n.205C=
ENST00000542067.5:c.359C=	ENSP00000438329.1:p.Pro120=
ENST00000543171.5:c.359C=	ENSP00000438131.2:p.Pro120=
ENST00000543318.5:c.359C=	ENSP00000444274.1:p.Pro120=
ENST00000543430.5:n.407C=
ENST00000543984.5:c.*52C=	ENSP00000439386.1:n.*52C=
NM_001256796.1:c.407C=	NP_001243725.1:p.Pro136=
NM_001261397.1:c.359C=	NP_001248326.1:p.Pro120=
NM_001261398.1:c.359C=	NP_001248327.1:p.Pro120=
NM_002560.2:c.359C=	NP_002551.2:p.Pro120=
NR_046372.1:n.663C=
NR_046373.1:n.515C=
XM_011538416.1:c.135-6435C=	XP_011536718.1:n.135-6435C=
XM_011538417.1:c.407C=	XP_011536719.1:p.Pro136=
XR_944559.1:n.467C=
XM_011538416.2:c.135-6435C=	XP_011536718.1:n.135-6435C=
XR_001748726.2:n.413C=
XR_001748727.1:n.476C=
XR_001748728.1:n.476C=
XR_001748729.2:n.413C=
XR_944559.2:n.466C=
NM_001256796.2:c.407C=	NP_001243725.1:p.Pro136=
NM_001261397.2:c.359C=	NP_001248326.1:p.Pro120=
NM_001261398.2:c.359C=	NP_001248327.1:p.Pro120=
NM_002560.3:c.359C= MANE Select	NP_002551.2:p.Pro120=
NR_046372.2:n.395C=
NR_046373.2:n.247C=