Canonical Allele Identifier: CA2067739911

Gene: P2RX4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121222151G= , CM000674.2:g.121222151G=	GRCh38
NC_000012.11:g.121659954G= , CM000674.1:g.121659954G=	GRCh37
NC_000012.10:g.120144337G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337233.9:c.412G= MANE Select	ENSP00000336607.4:p.Gly138=
ENST00000314442.7:n.4546G=
ENST00000337233.8:c.412G=	ENSP00000336607.4:p.Gly138=
ENST00000359949.11:c.460G=	ENSP00000353032.7:p.Gly154=
ENST00000499638.6:n.448G=
ENST00000538417.2:c.342G=
ENST00000538701.5:c.135-6382G=	ENSP00000444033.1:n.135-6382G=
ENST00000540930.5:n.448G=
ENST00000541187.5:n.258G=
ENST00000542067.5:c.412G=	ENSP00000438329.1:p.Gly138=
ENST00000543171.5:c.412G=	ENSP00000438131.2:p.Gly138=
ENST00000543318.5:c.412G=	ENSP00000444274.1:p.Gly138=
ENST00000543430.5:n.460G=
ENST00000543984.5:c.*105G=	ENSP00000439386.1:n.*105G=
NM_001256796.1:c.460G=	NP_001243725.1:p.Gly154=
NM_001261397.1:c.412G=	NP_001248326.1:p.Gly138=
NM_001261398.1:c.412G=	NP_001248327.1:p.Gly138=
NM_002560.2:c.412G=	NP_002551.2:p.Gly138=
NR_046372.1:n.716G=
NR_046373.1:n.568G=
XM_011538416.1:c.135-6382G=	XP_011536718.1:n.135-6382G=
XM_011538417.1:c.460G=	XP_011536719.1:p.Gly154=
XR_944559.1:n.520G=
XM_011538416.2:c.135-6382G=	XP_011536718.1:n.135-6382G=
XR_001748726.2:n.466G=
XR_001748727.1:n.529G=
XR_001748728.1:n.529G=
XR_001748729.2:n.466G=
XR_944559.2:n.519G=
NM_001256796.2:c.460G=	NP_001243725.1:p.Gly154=
NM_001261397.2:c.412G=	NP_001248326.1:p.Gly138=
NM_001261398.2:c.412G=	NP_001248327.1:p.Gly138=
NM_002560.3:c.412G= MANE Select	NP_002551.2:p.Gly138=
NR_046372.2:n.448G=
NR_046373.2:n.300G=