Canonical Allele Identifier: CA482157227

Gene: P2RX4

Linked Data

• MyVariant Identifiers: chr12:g.121659941T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121222138T>A , CM000674.2:g.121222138T>A	GRCh38
NC_000012.11:g.121659941T>A , CM000674.1:g.121659941T>A	GRCh37
NC_000012.10:g.120144324T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337233.9:c.399T>A MANE Select	ENSP00000336607.4:p.Thr133=
ENST00000314442.7:n.4533T>A
ENST00000337233.8:c.399T>A	ENSP00000336607.4:p.Thr133=
ENST00000359949.11:c.447T>A	ENSP00000353032.7:p.Thr149=
ENST00000499638.6:n.435T>A
ENST00000538417.2:c.329T>A
ENST00000538701.5:c.135-6395T>A	ENSP00000444033.1:n.135-6395T>A
ENST00000540930.5:n.435T>A
ENST00000541187.5:n.245T>A
ENST00000542067.5:c.399T>A	ENSP00000438329.1:p.Thr133=
ENST00000543171.5:c.399T>A	ENSP00000438131.2:p.Thr133=
ENST00000543318.5:c.399T>A	ENSP00000444274.1:p.Thr133=
ENST00000543430.5:n.447T>A
ENST00000543984.5:c.*92T>A	ENSP00000439386.1:n.*92T>A
NM_001256796.1:c.447T>A	NP_001243725.1:p.Thr149=
NM_001261397.1:c.399T>A	NP_001248326.1:p.Thr133=
NM_001261398.1:c.399T>A	NP_001248327.1:p.Thr133=
NM_002560.2:c.399T>A	NP_002551.2:p.Thr133=
NR_046372.1:n.703T>A
NR_046373.1:n.555T>A
XM_011538416.1:c.135-6395T>A	XP_011536718.1:n.135-6395T>A
XM_011538417.1:c.447T>A	XP_011536719.1:p.Thr149=
XR_944559.1:n.507T>A
XM_011538416.2:c.135-6395T>A	XP_011536718.1:n.135-6395T>A
XR_001748726.2:n.453T>A
XR_001748727.1:n.516T>A
XR_001748728.1:n.516T>A
XR_001748729.2:n.453T>A
XR_944559.2:n.506T>A
NM_001256796.2:c.447T>A	NP_001243725.1:p.Thr149=
NM_001261397.2:c.399T>A	NP_001248326.1:p.Thr133=
NM_001261398.2:c.399T>A	NP_001248327.1:p.Thr133=
NM_002560.3:c.399T>A MANE Select	NP_002551.2:p.Thr133=
NR_046372.2:n.435T>A
NR_046373.2:n.287T>A