Canonical Allele Identifier: CA386948602

Gene: P2RX4

Linked Data

• MyVariant Identifiers: chr12:g.121659971T>C (hg19) ; chr12:g.121222168T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121222168T>C , CM000674.2:g.121222168T>C	GRCh38
NC_000012.11:g.121659971T>C , CM000674.1:g.121659971T>C	GRCh37
NC_000012.10:g.120144354T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337233.9:c.427+2T>C MANE Select	ENSP00000336607.4:n.427+2T>C
ENST00000314442.7:n.4561+2T>C
ENST00000337233.8:c.427+2T>C	ENSP00000336607.4:n.427+2T>C
ENST00000359949.11:c.475+2T>C	ENSP00000353032.7:n.475+2T>C
ENST00000499638.6:n.465T>C
ENST00000538417.2:c.357+2T>C
ENST00000538701.5:c.135-6365T>C	ENSP00000444033.1:n.135-6365T>C
ENST00000540930.5:n.463+2T>C
ENST00000541187.5:n.273+2T>C
ENST00000542067.5:c.427+2T>C	ENSP00000438329.1:n.427+2T>C
ENST00000543171.5:c.427+2T>C	ENSP00000438131.2:n.427+2T>C
ENST00000543318.5:c.427+2T>C	ENSP00000444274.1:n.427+2T>C
ENST00000543430.5:n.475+2T>C
ENST00000543984.5:c.*120+2T>C	ENSP00000439386.1:n.*120+2T>C
NM_001256796.1:c.475+2T>C	NP_001243725.1:n.475+2T>C
NM_001261397.1:c.427+2T>C	NP_001248326.1:n.427+2T>C
NM_001261398.1:c.427+2T>C	NP_001248327.1:n.427+2T>C
NM_002560.2:c.427+2T>C	NP_002551.2:n.427+2T>C
NR_046372.1:n.731+2T>C
NR_046373.1:n.583+2T>C
XM_011538416.1:c.135-6365T>C	XP_011536718.1:n.135-6365T>C
XM_011538417.1:c.475+2T>C	XP_011536719.1:n.475+2T>C
XR_944559.1:n.535+2T>C
XM_011538416.2:c.135-6365T>C	XP_011536718.1:n.135-6365T>C
XR_001748726.2:n.481+2T>C
XR_001748727.1:n.544+2T>C
XR_001748728.1:n.544+2T>C
XR_001748729.2:n.481+2T>C
XR_944559.2:n.534+2T>C
NM_001256796.2:c.475+2T>C	NP_001243725.1:n.475+2T>C
NM_001261397.2:c.427+2T>C	NP_001248326.1:n.427+2T>C
NM_001261398.2:c.427+2T>C	NP_001248327.1:n.427+2T>C
NM_002560.3:c.427+2T>C MANE Select	NP_002551.2:n.427+2T>C
NR_046372.2:n.463+2T>C
NR_046373.2:n.315+2T>C