Canonical Allele Identifier: CA2067789596

Gene: P2RX4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121232482G= , CM000674.2:g.121232482G=	GRCh38
NC_000012.11:g.121670285G= , CM000674.1:g.121670285G=	GRCh37
NC_000012.10:g.120154668G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000337233.9:c.953G= MANE Select	ENSP00000336607.4:p.Arg318=
ENST00000337233.8:c.953G=	ENSP00000336607.4:p.Arg318=
ENST00000359949.11:c.1001G=	ENSP00000353032.7:p.Arg334=
ENST00000499638.6:n.1946G=
ENST00000538417.2:c.840G=
ENST00000541187.5:n.798G=
ENST00000542067.5:c.872G=	ENSP00000438329.1:p.Arg291=
ENST00000543171.5:c.953G=	ENSP00000438131.2:p.Arg318=
ENST00000543318.5:c.*544G=	ENSP00000444274.1:n.*544G=
ENST00000543430.5:n.904G=
ENST00000543984.5:c.*646G=	ENSP00000439386.1:n.*646G=
NM_001256796.1:c.1001G=	NP_001243725.1:p.Arg334=
NM_001261397.1:c.872G=	NP_001248326.1:p.Arg291=
NM_001261398.1:c.953G=	NP_001248327.1:p.Arg318=
NM_002560.2:c.953G=	NP_002551.2:p.Arg318=
NR_046372.1:n.1295G=
NR_046373.1:n.1109G=
XM_011538416.1:c.563G=	XP_011536718.1:p.Arg188=
XR_944559.1:n.990G=
XM_011538416.2:c.563G=	XP_011536718.1:p.Arg188=
XR_001748726.2:n.936G=
XR_001748727.1:n.1085G=
XR_001748728.1:n.1014G=
XR_001748729.2:n.1022G=
XR_944559.2:n.989G=
NM_001256796.2:c.1001G=	NP_001243725.1:p.Arg334=
NM_001261397.2:c.872G=	NP_001248326.1:p.Arg291=
NM_001261398.2:c.953G=	NP_001248327.1:p.Arg318=
NM_002560.3:c.953G= MANE Select	NP_002551.2:p.Arg318=
NR_046372.2:n.1027G=
NR_046373.2:n.841G=