Canonical Allele Identifier: CA2067789538

Gene: P2RX4

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000337233.9:c.885-30C= MANE Select	ENSP00000336607.4:n.885-30C=
ENST00000337233.8:c.885-30C=	ENSP00000336607.4:n.885-30C=
ENST00000359949.11:c.933-30C=	ENSP00000353032.7:n.933-30C=
ENST00000499638.6:n.1878-30C=
ENST00000538417.2:c.742C=
ENST00000541187.5:n.730-30C=
ENST00000542067.5:c.804-30C=	ENSP00000438329.1:n.804-30C=
ENST00000543171.5:c.885-30C=	ENSP00000438131.2:n.885-30C=
ENST00000543318.5:c.*476-30C=	ENSP00000444274.1:n.*476-30C=
ENST00000543430.5:n.836-30C=
ENST00000543984.5:c.*578-30C=	ENSP00000439386.1:n.*578-30C=
NM_001256796.1:c.933-30C=	NP_001243725.1:n.933-30C=
NM_001261397.1:c.804-30C=	NP_001248326.1:n.804-30C=
NM_001261398.1:c.885-30C=	NP_001248327.1:n.885-30C=
NM_002560.2:c.885-30C=	NP_002551.2:n.885-30C=
NR_046372.1:n.1227-30C=
NR_046373.1:n.1041-30C=
XM_011538416.1:c.495-30C=	XP_011536718.1:n.495-30C=
XR_944559.1:n.922-30C=
XM_011538416.2:c.495-30C=	XP_011536718.1:n.495-30C=
XR_001748726.2:n.868-30C=
XR_001748727.1:n.1017-30C=
XR_001748728.1:n.946-30C=
XR_001748729.2:n.954-30C=
XR_944559.2:n.921-30C=
NM_001256796.2:c.933-30C=	NP_001243725.1:n.933-30C=
NM_001261397.2:c.804-30C=	NP_001248326.1:n.804-30C=
NM_001261398.2:c.885-30C=	NP_001248327.1:n.885-30C=
NM_002560.3:c.885-30C= MANE Select	NP_002551.2:n.885-30C=
NR_046372.2:n.959-30C=
NR_046373.2:n.773-30C=