Canonical Allele Identifier: CA244556132

Gene: P2RX4

Linked Data

• dbSNP Id: rs992689660
• MyVariant Identifiers: chr12:g.121659851T>G (hg19) ; chr12:g.121222048T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121222048T>G , CM000674.2:g.121222048T>G	GRCh38
NC_000012.11:g.121659851T>G , CM000674.1:g.121659851T>G	GRCh37
NC_000012.10:g.120144234T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000337233.9:c.355-46T>G MANE Select	ENSP00000336607.4:n.355-46T>G
ENST00000314442.7:n.4489-46T>G
ENST00000337233.8:c.355-46T>G	ENSP00000336607.4:n.355-46T>G
ENST00000359949.11:c.403-46T>G	ENSP00000353032.7:n.403-46T>G
ENST00000499638.6:n.391-46T>G
ENST00000538417.2:c.285-46T>G
ENST00000538701.5:c.135-6485T>G	ENSP00000444033.1:n.135-6485T>G
ENST00000540930.5:n.391-46T>G
ENST00000541187.5:n.201-46T>G
ENST00000542067.5:c.355-46T>G	ENSP00000438329.1:n.355-46T>G
ENST00000543171.5:c.355-46T>G	ENSP00000438131.2:n.355-46T>G
ENST00000543318.5:c.355-46T>G	ENSP00000444274.1:n.355-46T>G
ENST00000543430.5:n.403-46T>G
ENST00000543984.5:c.*48-46T>G	ENSP00000439386.1:n.*48-46T>G
NM_001256796.1:c.403-46T>G	NP_001243725.1:n.403-46T>G
NM_001261397.1:c.355-46T>G	NP_001248326.1:n.355-46T>G
NM_001261398.1:c.355-46T>G	NP_001248327.1:n.355-46T>G
NM_002560.2:c.355-46T>G	NP_002551.2:n.355-46T>G
NR_046372.1:n.659-46T>G
NR_046373.1:n.511-46T>G
XM_011538416.1:c.135-6485T>G	XP_011536718.1:n.135-6485T>G
XM_011538417.1:c.403-46T>G	XP_011536719.1:n.403-46T>G
XR_944559.1:n.463-46T>G
XM_011538416.2:c.135-6485T>G	XP_011536718.1:n.135-6485T>G
XR_001748726.2:n.409-46T>G
XR_001748727.1:n.472-46T>G
XR_001748728.1:n.472-46T>G
XR_001748729.2:n.409-46T>G
XR_944559.2:n.462-46T>G
NM_001256796.2:c.403-46T>G	NP_001243725.1:n.403-46T>G
NM_001261397.2:c.355-46T>G	NP_001248326.1:n.355-46T>G
NM_001261398.2:c.355-46T>G	NP_001248327.1:n.355-46T>G
NM_002560.3:c.355-46T>G MANE Select	NP_002551.2:n.355-46T>G
NR_046372.2:n.391-46T>G
NR_046373.2:n.243-46T>G