Canonical Allele Identifier: CA2797733421

Gene: P2RX4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121221954del , CM000674.2:g.121221954del	GRCh38
NC_000012.11:g.121659757del , CM000674.1:g.121659757del	GRCh37
NC_000012.10:g.120144140del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337233.9:c.324del MANE Select	ENSP00000336607.4:p.Met109Ter
ENST00000314442.7:n.4458del
ENST00000337233.8:c.324del	ENSP00000336607.4:p.Met109Ter
ENST00000359949.11:c.372del	ENSP00000353032.7:p.Met125Ter
ENST00000499638.6:n.360del
ENST00000538417.2:c.254del
ENST00000538701.5:c.135-6579del	ENSP00000444033.1:n.135-6579del
ENST00000540930.5:n.360del
ENST00000541187.5:n.170del
ENST00000542067.5:c.324del	ENSP00000438329.1:p.Met109Ter
ENST00000543171.5:c.324del	ENSP00000438131.2:p.Met109Ter
ENST00000543318.5:c.324del	ENSP00000444274.1:p.Met109Ter
ENST00000543430.5:n.372del
ENST00000543984.5:c.*17del	ENSP00000439386.1:n.*17del
NM_001256796.1:c.372del	NP_001243725.1:p.Met125Ter
NM_001261397.1:c.324del	NP_001248326.1:p.Met109Ter
NM_001261398.1:c.324del	NP_001248327.1:p.Met109Ter
NM_002560.2:c.324del	NP_002551.2:p.Met109Ter
NR_046372.1:n.628del
NR_046373.1:n.480del
XM_011538416.1:c.135-6579del	XP_011536718.1:n.135-6579del
XM_011538417.1:c.372del	XP_011536719.1:p.Met125Ter
XR_944559.1:n.432del
XM_011538416.2:c.135-6579del	XP_011536718.1:n.135-6579del
XR_001748726.2:n.378del
XR_001748727.1:n.441del
XR_001748728.1:n.441del
XR_001748729.2:n.378del
XR_944559.2:n.431del
NM_001256796.2:c.372del	NP_001243725.1:p.Met125Ter
NM_001261397.2:c.324del	NP_001248326.1:p.Met109Ter
NM_001261398.2:c.324del	NP_001248327.1:p.Met109Ter
NM_002560.3:c.324del MANE Select	NP_002551.2:p.Met109Ter
NR_046372.2:n.360del
NR_046373.2:n.212del