Canonical Allele Identifier: CA2067739865

Gene: P2RX4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121222127G= , CM000674.2:g.121222127G=	GRCh38
NC_000012.11:g.121659930G= , CM000674.1:g.121659930G=	GRCh37
NC_000012.10:g.120144313G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337233.9:c.388G= MANE Select	ENSP00000336607.4:p.Ala130=
ENST00000314442.7:n.4522G=
ENST00000337233.8:c.388G=	ENSP00000336607.4:p.Ala130=
ENST00000359949.11:c.436G=	ENSP00000353032.7:p.Ala146=
ENST00000499638.6:n.424G=
ENST00000538417.2:c.318G=
ENST00000538701.5:c.135-6406G=	ENSP00000444033.1:n.135-6406G=
ENST00000540930.5:n.424G=
ENST00000541187.5:n.234G=
ENST00000542067.5:c.388G=	ENSP00000438329.1:p.Ala130=
ENST00000543171.5:c.388G=	ENSP00000438131.2:p.Ala130=
ENST00000543318.5:c.388G=	ENSP00000444274.1:p.Ala130=
ENST00000543430.5:n.436G=
ENST00000543984.5:c.*81G=	ENSP00000439386.1:n.*81G=
NM_001256796.1:c.436G=	NP_001243725.1:p.Ala146=
NM_001261397.1:c.388G=	NP_001248326.1:p.Ala130=
NM_001261398.1:c.388G=	NP_001248327.1:p.Ala130=
NM_002560.2:c.388G=	NP_002551.2:p.Ala130=
NR_046372.1:n.692G=
NR_046373.1:n.544G=
XM_011538416.1:c.135-6406G=	XP_011536718.1:n.135-6406G=
XM_011538417.1:c.436G=	XP_011536719.1:p.Ala146=
XR_944559.1:n.496G=
XM_011538416.2:c.135-6406G=	XP_011536718.1:n.135-6406G=
XR_001748726.2:n.442G=
XR_001748727.1:n.505G=
XR_001748728.1:n.505G=
XR_001748729.2:n.442G=
XR_944559.2:n.495G=
NM_001256796.2:c.436G=	NP_001243725.1:p.Ala146=
NM_001261397.2:c.388G=	NP_001248326.1:p.Ala130=
NM_001261398.2:c.388G=	NP_001248327.1:p.Ala130=
NM_002560.3:c.388G= MANE Select	NP_002551.2:p.Ala130=
NR_046372.2:n.424G=
NR_046373.2:n.276G=