Canonical Allele Identifier: CA2067739627

Gene: P2RX4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121222031G= , CM000674.2:g.121222031G=	GRCh38
NC_000012.11:g.121659834G= , CM000674.1:g.121659834G=	GRCh37
NC_000012.10:g.120144217G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337233.9:c.354+47G= MANE Select	ENSP00000336607.4:n.354+47G=
ENST00000314442.7:n.4488+47G=
ENST00000337233.8:c.354+47G=	ENSP00000336607.4:n.354+47G=
ENST00000359949.11:c.402+47G=	ENSP00000353032.7:n.402+47G=
ENST00000499638.6:n.390+47G=
ENST00000538417.2:c.284+47G=
ENST00000538701.5:c.135-6502G=	ENSP00000444033.1:n.135-6502G=
ENST00000540930.5:n.390+47G=
ENST00000541187.5:n.200+47G=
ENST00000542067.5:c.354+47G=	ENSP00000438329.1:n.354+47G=
ENST00000543171.5:c.354+47G=	ENSP00000438131.2:n.354+47G=
ENST00000543318.5:c.354+47G=	ENSP00000444274.1:n.354+47G=
ENST00000543430.5:n.402+47G=
ENST00000543984.5:c.*47+47G=	ENSP00000439386.1:n.*47+47G=
NM_001256796.1:c.402+47G=	NP_001243725.1:n.402+47G=
NM_001261397.1:c.354+47G=	NP_001248326.1:n.354+47G=
NM_001261398.1:c.354+47G=	NP_001248327.1:n.354+47G=
NM_002560.2:c.354+47G=	NP_002551.2:n.354+47G=
NR_046372.1:n.658+47G=
NR_046373.1:n.510+47G=
XM_011538416.1:c.135-6502G=	XP_011536718.1:n.135-6502G=
XM_011538417.1:c.402+47G=	XP_011536719.1:n.402+47G=
XR_944559.1:n.462+47G=
XM_011538416.2:c.135-6502G=	XP_011536718.1:n.135-6502G=
XR_001748726.2:n.408+47G=
XR_001748727.1:n.471+47G=
XR_001748728.1:n.471+47G=
XR_001748729.2:n.408+47G=
XR_944559.2:n.461+47G=
NM_001256796.2:c.402+47G=	NP_001243725.1:n.402+47G=
NM_001261397.2:c.354+47G=	NP_001248326.1:n.354+47G=
NM_001261398.2:c.354+47G=	NP_001248327.1:n.354+47G=
NM_002560.3:c.354+47G= MANE Select	NP_002551.2:n.354+47G=
NR_046372.2:n.390+47G=
NR_046373.2:n.242+47G=