Canonical Allele Identifier: CA2067739897

Gene: P2RX4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121222145T= , CM000674.2:g.121222145T=	GRCh38
NC_000012.11:g.121659948T= , CM000674.1:g.121659948T=	GRCh37
NC_000012.10:g.120144331T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337233.9:c.406T= MANE Select	ENSP00000336607.4:p.Ser136=
ENST00000314442.7:n.4540T=
ENST00000337233.8:c.406T=	ENSP00000336607.4:p.Ser136=
ENST00000359949.11:c.454T=	ENSP00000353032.7:p.Ser152=
ENST00000499638.6:n.442T=
ENST00000538417.2:c.336T=
ENST00000538701.5:c.135-6388T=	ENSP00000444033.1:n.135-6388T=
ENST00000540930.5:n.442T=
ENST00000541187.5:n.252T=
ENST00000542067.5:c.406T=	ENSP00000438329.1:p.Ser136=
ENST00000543171.5:c.406T=	ENSP00000438131.2:p.Ser136=
ENST00000543318.5:c.406T=	ENSP00000444274.1:p.Ser136=
ENST00000543430.5:n.454T=
ENST00000543984.5:c.*99T=	ENSP00000439386.1:n.*99T=
NM_001256796.1:c.454T=	NP_001243725.1:p.Ser152=
NM_001261397.1:c.406T=	NP_001248326.1:p.Ser136=
NM_001261398.1:c.406T=	NP_001248327.1:p.Ser136=
NM_002560.2:c.406T=	NP_002551.2:p.Ser136=
NR_046372.1:n.710T=
NR_046373.1:n.562T=
XM_011538416.1:c.135-6388T=	XP_011536718.1:n.135-6388T=
XM_011538417.1:c.454T=	XP_011536719.1:p.Ser152=
XR_944559.1:n.514T=
XM_011538416.2:c.135-6388T=	XP_011536718.1:n.135-6388T=
XR_001748726.2:n.460T=
XR_001748727.1:n.523T=
XR_001748728.1:n.523T=
XR_001748729.2:n.460T=
XR_944559.2:n.513T=
NM_001256796.2:c.454T=	NP_001243725.1:p.Ser152=
NM_001261397.2:c.406T=	NP_001248326.1:p.Ser136=
NM_001261398.2:c.406T=	NP_001248327.1:p.Ser136=
NM_002560.3:c.406T= MANE Select	NP_002551.2:p.Ser136=
NR_046372.2:n.442T=
NR_046373.2:n.294T=