Canonical Allele Identifier: CA6833935

Gene: P2RX4

Linked Data

• dbSNP Id: rs369148862
• ExAC: 12:121659953 C / T
• gnomAD v2: 12-121659953-C-T
• gnomAD v3: 12-121222150-C-T
• gnomAD v4: 12-121222150-C-T
• MyVariant Identifiers: chr12:g.121659953C>T (hg19) ; chr12:g.121222150C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121222150C>T , CM000674.2:g.121222150C>T	GRCh38
NC_000012.11:g.121659953C>T , CM000674.1:g.121659953C>T	GRCh37
NC_000012.10:g.120144336C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000337233.9:c.411C>T MANE Select	ENSP00000336607.4:p.Ala137=
ENST00000314442.7:n.4545C>T
ENST00000337233.8:c.411C>T	ENSP00000336607.4:p.Ala137=
ENST00000359949.11:c.459C>T	ENSP00000353032.7:p.Ala153=
ENST00000499638.6:n.447C>T
ENST00000538417.2:c.341C>T
ENST00000538701.5:c.135-6383C>T	ENSP00000444033.1:n.135-6383C>T
ENST00000540930.5:n.447C>T
ENST00000541187.5:n.257C>T
ENST00000542067.5:c.411C>T	ENSP00000438329.1:p.Ala137=
ENST00000543171.5:c.411C>T	ENSP00000438131.2:p.Ala137=
ENST00000543318.5:c.411C>T	ENSP00000444274.1:p.Ala137=
ENST00000543430.5:n.459C>T
ENST00000543984.5:c.*104C>T	ENSP00000439386.1:n.*104C>T
NM_001256796.1:c.459C>T	NP_001243725.1:p.Ala153=
NM_001261397.1:c.411C>T	NP_001248326.1:p.Ala137=
NM_001261398.1:c.411C>T	NP_001248327.1:p.Ala137=
NM_002560.2:c.411C>T	NP_002551.2:p.Ala137=
NR_046372.1:n.715C>T
NR_046373.1:n.567C>T
XM_011538416.1:c.135-6383C>T	XP_011536718.1:n.135-6383C>T
XM_011538417.1:c.459C>T	XP_011536719.1:p.Ala153=
XR_944559.1:n.519C>T
XM_011538416.2:c.135-6383C>T	XP_011536718.1:n.135-6383C>T
XR_001748726.2:n.465C>T
XR_001748727.1:n.528C>T
XR_001748728.1:n.528C>T
XR_001748729.2:n.465C>T
XR_944559.2:n.518C>T
NM_001256796.2:c.459C>T	NP_001243725.1:p.Ala153=
NM_001261397.2:c.411C>T	NP_001248326.1:p.Ala137=
NM_001261398.2:c.411C>T	NP_001248327.1:p.Ala137=
NM_002560.3:c.411C>T MANE Select	NP_002551.2:p.Ala137=
NR_046372.2:n.447C>T
NR_046373.2:n.299C>T