Canonical Allele Identifier: CA2067739025

Gene: P2RX4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121221712T= , CM000674.2:g.121221712T=	GRCh38
NC_000012.11:g.121659515T= , CM000674.1:g.121659515T=	GRCh37
NC_000012.10:g.120143898T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337233.9:c.283-201T= MANE Select	ENSP00000336607.4:n.283-201T=
ENST00000314442.7:n.4417-201T=
ENST00000337233.8:c.283-201T=	ENSP00000336607.4:n.283-201T=
ENST00000359949.11:c.331-201T=	ENSP00000353032.7:n.331-201T=
ENST00000499638.6:n.319-201T=
ENST00000538417.2:c.213-201T=
ENST00000538701.5:c.135-6821T=	ENSP00000444033.1:n.135-6821T=
ENST00000540930.5:n.319-201T=
ENST00000541187.5:n.129-201T=
ENST00000542067.5:c.283-201T=	ENSP00000438329.1:n.283-201T=
ENST00000543171.5:c.283-201T=	ENSP00000438131.2:n.283-201T=
ENST00000543318.5:c.283-201T=	ENSP00000444274.1:n.283-201T=
ENST00000543430.5:n.331-201T=
ENST00000543984.5:c.135-201T=	ENSP00000439386.1:n.135-201T=
NM_001256796.1:c.331-201T=	NP_001243725.1:n.331-201T=
NM_001261397.1:c.283-201T=	NP_001248326.1:n.283-201T=
NM_001261398.1:c.283-201T=	NP_001248327.1:n.283-201T=
NM_002560.2:c.283-201T=	NP_002551.2:n.283-201T=
NR_046372.1:n.587-201T=
NR_046373.1:n.439-201T=
XM_011538416.1:c.135-6821T=	XP_011536718.1:n.135-6821T=
XM_011538417.1:c.331-201T=	XP_011536719.1:n.331-201T=
XR_944559.1:n.391-201T=
XM_011538416.2:c.135-6821T=	XP_011536718.1:n.135-6821T=
XR_001748726.2:n.337-201T=
XR_001748727.1:n.400-201T=
XR_001748728.1:n.400-201T=
XR_001748729.2:n.337-201T=
XR_944559.2:n.390-201T=
NM_001256796.2:c.331-201T=	NP_001243725.1:n.331-201T=
NM_001261397.2:c.283-201T=	NP_001248326.1:n.283-201T=
NM_001261398.2:c.283-201T=	NP_001248327.1:n.283-201T=
NM_002560.3:c.283-201T= MANE Select	NP_002551.2:n.283-201T=
NR_046372.2:n.319-201T=
NR_046373.2:n.171-201T=