Canonical Allele Identifier: CA482157234

Gene: P2RX4

Linked Data

• gnomAD v4: 12-121222144-C-T
• MyVariant Identifiers: chr12:g.121659947C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121222144C>T , CM000674.2:g.121222144C>T	GRCh38
NC_000012.11:g.121659947C>T , CM000674.1:g.121659947C>T	GRCh37
NC_000012.10:g.120144330C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000337233.9:c.405C>T MANE Select	ENSP00000336607.4:p.Gly135=
ENST00000314442.7:n.4539C>T
ENST00000337233.8:c.405C>T	ENSP00000336607.4:p.Gly135=
ENST00000359949.11:c.453C>T	ENSP00000353032.7:p.Gly151=
ENST00000499638.6:n.441C>T
ENST00000538417.2:c.335C>T
ENST00000538701.5:c.135-6389C>T	ENSP00000444033.1:n.135-6389C>T
ENST00000540930.5:n.441C>T
ENST00000541187.5:n.251C>T
ENST00000542067.5:c.405C>T	ENSP00000438329.1:p.Gly135=
ENST00000543171.5:c.405C>T	ENSP00000438131.2:p.Gly135=
ENST00000543318.5:c.405C>T	ENSP00000444274.1:p.Gly135=
ENST00000543430.5:n.453C>T
ENST00000543984.5:c.*98C>T	ENSP00000439386.1:n.*98C>T
NM_001256796.1:c.453C>T	NP_001243725.1:p.Gly151=
NM_001261397.1:c.405C>T	NP_001248326.1:p.Gly135=
NM_001261398.1:c.405C>T	NP_001248327.1:p.Gly135=
NM_002560.2:c.405C>T	NP_002551.2:p.Gly135=
NR_046372.1:n.709C>T
NR_046373.1:n.561C>T
XM_011538416.1:c.135-6389C>T	XP_011536718.1:n.135-6389C>T
XM_011538417.1:c.453C>T	XP_011536719.1:p.Gly151=
XR_944559.1:n.513C>T
XM_011538416.2:c.135-6389C>T	XP_011536718.1:n.135-6389C>T
XR_001748726.2:n.459C>T
XR_001748727.1:n.522C>T
XR_001748728.1:n.522C>T
XR_001748729.2:n.459C>T
XR_944559.2:n.512C>T
NM_001256796.2:c.453C>T	NP_001243725.1:p.Gly151=
NM_001261397.2:c.405C>T	NP_001248326.1:p.Gly135=
NM_001261398.2:c.405C>T	NP_001248327.1:p.Gly135=
NM_002560.3:c.405C>T MANE Select	NP_002551.2:p.Gly135=
NR_046372.2:n.441C>T
NR_046373.2:n.293C>T