Canonical Allele Identifier: CA2575323153

Gene: P2RX4

Linked Data

• gnomAD v4: 12-121232387-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121232387C>T , CM000674.2:g.121232387C>T	GRCh38
NC_000012.11:g.121670190C>T , CM000674.1:g.121670190C>T	GRCh37
NC_000012.10:g.120154573C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000337233.9:c.885-27C>T MANE Select	ENSP00000336607.4:n.885-27C>T
ENST00000337233.8:c.885-27C>T	ENSP00000336607.4:n.885-27C>T
ENST00000359949.11:c.933-27C>T	ENSP00000353032.7:n.933-27C>T
ENST00000499638.6:n.1878-27C>T
ENST00000538417.2:c.745C>T
ENST00000541187.5:n.730-27C>T
ENST00000542067.5:c.804-27C>T	ENSP00000438329.1:n.804-27C>T
ENST00000543171.5:c.885-27C>T	ENSP00000438131.2:n.885-27C>T
ENST00000543318.5:c.*476-27C>T	ENSP00000444274.1:n.*476-27C>T
ENST00000543430.5:n.836-27C>T
ENST00000543984.5:c.*578-27C>T	ENSP00000439386.1:n.*578-27C>T
NM_001256796.1:c.933-27C>T	NP_001243725.1:n.933-27C>T
NM_001261397.1:c.804-27C>T	NP_001248326.1:n.804-27C>T
NM_001261398.1:c.885-27C>T	NP_001248327.1:n.885-27C>T
NM_002560.2:c.885-27C>T	NP_002551.2:n.885-27C>T
NR_046372.1:n.1227-27C>T
NR_046373.1:n.1041-27C>T
XM_011538416.1:c.495-27C>T	XP_011536718.1:n.495-27C>T
XR_944559.1:n.922-27C>T
XM_011538416.2:c.495-27C>T	XP_011536718.1:n.495-27C>T
XR_001748726.2:n.868-27C>T
XR_001748727.1:n.1017-27C>T
XR_001748728.1:n.946-27C>T
XR_001748729.2:n.954-27C>T
XR_944559.2:n.921-27C>T
NM_001256796.2:c.933-27C>T	NP_001243725.1:n.933-27C>T
NM_001261397.2:c.804-27C>T	NP_001248326.1:n.804-27C>T
NM_001261398.2:c.885-27C>T	NP_001248327.1:n.885-27C>T
NM_002560.3:c.885-27C>T MANE Select	NP_002551.2:n.885-27C>T
NR_046372.2:n.959-27C>T
NR_046373.2:n.773-27C>T