Canonical Allele Identifier: CA2067739816

Gene: P2RX4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121222105G= , CM000674.2:g.121222105G=	GRCh38
NC_000012.11:g.121659908G= , CM000674.1:g.121659908G=	GRCh37
NC_000012.10:g.120144291G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337233.9:c.366G= MANE Select	ENSP00000336607.4:p.Ala122=
ENST00000314442.7:n.4500G=
ENST00000337233.8:c.366G=	ENSP00000336607.4:p.Ala122=
ENST00000359949.11:c.414G=	ENSP00000353032.7:p.Ala138=
ENST00000499638.6:n.402G=
ENST00000538417.2:c.296G=
ENST00000538701.5:c.135-6428G=	ENSP00000444033.1:n.135-6428G=
ENST00000540930.5:n.402G=
ENST00000541187.5:n.212G=
ENST00000542067.5:c.366G=	ENSP00000438329.1:p.Ala122=
ENST00000543171.5:c.366G=	ENSP00000438131.2:p.Ala122=
ENST00000543318.5:c.366G=	ENSP00000444274.1:p.Ala122=
ENST00000543430.5:n.414G=
ENST00000543984.5:c.*59G=	ENSP00000439386.1:n.*59G=
NM_001256796.1:c.414G=	NP_001243725.1:p.Ala138=
NM_001261397.1:c.366G=	NP_001248326.1:p.Ala122=
NM_001261398.1:c.366G=	NP_001248327.1:p.Ala122=
NM_002560.2:c.366G=	NP_002551.2:p.Ala122=
NR_046372.1:n.670G=
NR_046373.1:n.522G=
XM_011538416.1:c.135-6428G=	XP_011536718.1:n.135-6428G=
XM_011538417.1:c.414G=	XP_011536719.1:p.Ala138=
XR_944559.1:n.474G=
XM_011538416.2:c.135-6428G=	XP_011536718.1:n.135-6428G=
XR_001748726.2:n.420G=
XR_001748727.1:n.483G=
XR_001748728.1:n.483G=
XR_001748729.2:n.420G=
XR_944559.2:n.473G=
NM_001256796.2:c.414G=	NP_001243725.1:p.Ala138=
NM_001261397.2:c.366G=	NP_001248326.1:p.Ala122=
NM_001261398.2:c.366G=	NP_001248327.1:p.Ala122=
NM_002560.3:c.366G= MANE Select	NP_002551.2:p.Ala122=
NR_046372.2:n.402G=
NR_046373.2:n.254G=