Canonical Allele Identifier: CA2067789539

Gene: P2RX4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121232384_121232385delinsCT , CM000674.2:g.121232384_121232385delinsCT	GRCh38
NC_000012.11:g.121670187_121670188delinsCT , CM000674.1:g.121670187_121670188delinsCT	GRCh37
NC_000012.10:g.120154570_120154571delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000337233.9:c.885-30_885-29delinsCT MANE Select	ENSP00000336607.4:n.885-30_885-29delinsCT
ENST00000337233.8:c.885-30_885-29delinsCT	ENSP00000336607.4:n.885-30_885-29delinsCT
ENST00000359949.11:c.933-30_933-29delinsCT	ENSP00000353032.7:n.933-30_933-29delinsCT
ENST00000499638.6:n.1878-30_1878-29delinsCT
ENST00000538417.2:c.742_743delinsCT
ENST00000541187.5:n.730-30_730-29delinsCT
ENST00000542067.5:c.804-30_804-29delinsCT	ENSP00000438329.1:n.804-30_804-29delinsCT
ENST00000543171.5:c.885-30_885-29delinsCT	ENSP00000438131.2:n.885-30_885-29delinsCT
ENST00000543318.5:c.*476-30_*476-29delinsCT	ENSP00000444274.1:n.*476-30_*476-29delinsCT
ENST00000543430.5:n.836-30_836-29delinsCT
ENST00000543984.5:c.*578-30_*578-29delinsCT	ENSP00000439386.1:n.*578-30_*578-29delinsCT
NM_001256796.1:c.933-30_933-29delinsCT	NP_001243725.1:n.933-30_933-29delinsCT
NM_001261397.1:c.804-30_804-29delinsCT	NP_001248326.1:n.804-30_804-29delinsCT
NM_001261398.1:c.885-30_885-29delinsCT	NP_001248327.1:n.885-30_885-29delinsCT
NM_002560.2:c.885-30_885-29delinsCT	NP_002551.2:n.885-30_885-29delinsCT
NR_046372.1:n.1227-30_1227-29delinsCT
NR_046373.1:n.1041-30_1041-29delinsCT
XM_011538416.1:c.495-30_495-29delinsCT	XP_011536718.1:n.495-30_495-29delinsCT
XR_944559.1:n.922-30_922-29delinsCT
XM_011538416.2:c.495-30_495-29delinsCT	XP_011536718.1:n.495-30_495-29delinsCT
XR_001748726.2:n.868-30_868-29delinsCT
XR_001748727.1:n.1017-30_1017-29delinsCT
XR_001748728.1:n.946-30_946-29delinsCT
XR_001748729.2:n.954-30_954-29delinsCT
XR_944559.2:n.921-30_921-29delinsCT
NM_001256796.2:c.933-30_933-29delinsCT	NP_001243725.1:n.933-30_933-29delinsCT
NM_001261397.2:c.804-30_804-29delinsCT	NP_001248326.1:n.804-30_804-29delinsCT
NM_001261398.2:c.885-30_885-29delinsCT	NP_001248327.1:n.885-30_885-29delinsCT
NM_002560.3:c.885-30_885-29delinsCT MANE Select	NP_002551.2:n.885-30_885-29delinsCT
NR_046372.2:n.959-30_959-29delinsCT
NR_046373.2:n.773-30_773-29delinsCT