Canonical Allele Identifier: CA386947759

Gene: P2RX4

Linked Data

• MyVariant Identifiers: chr12:g.121659735T>C (hg19) ; chr12:g.121221932T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121221932T>C , CM000674.2:g.121221932T>C	GRCh38
NC_000012.11:g.121659735T>C , CM000674.1:g.121659735T>C	GRCh37
NC_000012.10:g.120144118T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337233.9:c.302T>C MANE Select	ENSP00000336607.4:p.Val101Ala
ENST00000314442.7:n.4436T>C
ENST00000337233.8:c.302T>C	ENSP00000336607.4:p.Val101Ala
ENST00000359949.11:c.350T>C	ENSP00000353032.7:p.Val117Ala
ENST00000499638.6:n.338T>C
ENST00000538417.2:c.232T>C
ENST00000538701.5:c.135-6601T>C	ENSP00000444033.1:n.135-6601T>C
ENST00000540930.5:n.338T>C
ENST00000541187.5:n.148T>C
ENST00000542067.5:c.302T>C	ENSP00000438329.1:p.Val101Ala
ENST00000543171.5:c.302T>C	ENSP00000438131.2:p.Val101Ala
ENST00000543318.5:c.302T>C	ENSP00000444274.1:p.Val101Ala
ENST00000543430.5:n.350T>C
ENST00000543984.5:c.154T>C	ENSP00000439386.1:p.Ser52Pro
NM_001256796.1:c.350T>C	NP_001243725.1:p.Val117Ala
NM_001261397.1:c.302T>C	NP_001248326.1:p.Val101Ala
NM_001261398.1:c.302T>C	NP_001248327.1:p.Val101Ala
NM_002560.2:c.302T>C	NP_002551.2:p.Val101Ala
NR_046372.1:n.606T>C
NR_046373.1:n.458T>C
XM_011538416.1:c.135-6601T>C	XP_011536718.1:n.135-6601T>C
XM_011538417.1:c.350T>C	XP_011536719.1:p.Val117Ala
XR_944559.1:n.410T>C
XM_011538416.2:c.135-6601T>C	XP_011536718.1:n.135-6601T>C
XR_001748726.2:n.356T>C
XR_001748727.1:n.419T>C
XR_001748728.1:n.419T>C
XR_001748729.2:n.356T>C
XR_944559.2:n.409T>C
NM_001256796.2:c.350T>C	NP_001243725.1:p.Val117Ala
NM_001261397.2:c.302T>C	NP_001248326.1:p.Val101Ala
NM_001261398.2:c.302T>C	NP_001248327.1:p.Val101Ala
NM_002560.3:c.302T>C MANE Select	NP_002551.2:p.Val101Ala
NR_046372.2:n.338T>C
NR_046373.2:n.190T>C