Canonical Allele Identifier: CA2067739993

Gene: P2RX4

Linked Data

• dbSNP Id: rs1886663264

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121222195_121222196insAGCTCCTGGGGAGGGC , CM000674.2:g.121222195_121222196insAGCTCCTGGGGAGGGC	GRCh38
NC_000012.11:g.121659998_121659999insAGCTCCTGGGGAGGGC , CM000674.1:g.121659998_121659999insAGCTCCTGGGGAGGGC	GRCh37
NC_000012.10:g.120144381_120144382insAGCTCCTGGGGAGGGC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337233.9:c.427+29_427+30insAGCTCCTGGGGAGGGC MANE Select	ENSP00000336607.4:n.427+29_427+30insAGCTCCTGGGGAGGGC
ENST00000314442.7:n.4561+29_4561+30insAGCTCCTGGGGAGGGC
ENST00000337233.8:c.427+29_427+30insAGCTCCTGGGGAGGGC	ENSP00000336607.4:n.427+29_427+30insAGCTCCTGGGGAGGGC
ENST00000359949.11:c.475+29_475+30insAGCTCCTGGGGAGGGC	ENSP00000353032.7:n.475+29_475+30insAGCTCCTGGGGAGGGC
ENST00000499638.6:n.492_493insAGCTCCTGGGGAGGGC
ENST00000538417.2:c.357+29_357+30insAGCTCCTGGGGAGGGC
ENST00000538701.5:c.135-6338_135-6337insAGCTCCTGGGGAGGGC	ENSP00000444033.1:n.135-6338_135-6337insAGCTCCTGGGGAGGGC
ENST00000540930.5:n.463+29_463+30insAGCTCCTGGGGAGGGC
ENST00000541187.5:n.273+29_273+30insAGCTCCTGGGGAGGGC
ENST00000542067.5:c.427+29_427+30insAGCTCCTGGGGAGGGC	ENSP00000438329.1:n.427+29_427+30insAGCTCCTGGGGAGGGC
ENST00000543171.5:c.427+29_427+30insAGCTCCTGGGGAGGGC	ENSP00000438131.2:n.427+29_427+30insAGCTCCTGGGGAGGGC
ENST00000543318.5:c.427+29_427+30insAGCTCCTGGGGAGGGC	ENSP00000444274.1:n.427+29_427+30insAGCTCCTGGGGAGGGC
ENST00000543430.5:n.475+29_475+30insAGCTCCTGGGGAGGGC
ENST00000543984.5:c.*120+29_*120+30insAGCTCCTGGGGAGGGC	ENSP00000439386.1:n.*120+29_*120+30insAGCTCCTGGGGAGGGC
NM_001256796.1:c.475+29_475+30insAGCTCCTGGGGAGGGC	NP_001243725.1:n.475+29_475+30insAGCTCCTGGGGAGGGC
NM_001261397.1:c.427+29_427+30insAGCTCCTGGGGAGGGC	NP_001248326.1:n.427+29_427+30insAGCTCCTGGGGAGGGC
NM_001261398.1:c.427+29_427+30insAGCTCCTGGGGAGGGC	NP_001248327.1:n.427+29_427+30insAGCTCCTGGGGAGGGC
NM_002560.2:c.427+29_427+30insAGCTCCTGGGGAGGGC	NP_002551.2:n.427+29_427+30insAGCTCCTGGGGAGGGC
NR_046372.1:n.731+29_731+30insAGCTCCTGGGGAGGGC
NR_046373.1:n.583+29_583+30insAGCTCCTGGGGAGGGC
XM_011538416.1:c.135-6338_135-6337insAGCTCCTGGGGAGGGC	XP_011536718.1:n.135-6338_135-6337insAGCTCCTGGGGAGGGC
XM_011538417.1:c.475+29_475+30insAGCTCCTGGGGAGGGC	XP_011536719.1:n.475+29_475+30insAGCTCCTGGGGAGGGC
XR_944559.1:n.535+29_535+30insAGCTCCTGGGGAGGGC
XM_011538416.2:c.135-6338_135-6337insAGCTCCTGGGGAGGGC	XP_011536718.1:n.135-6338_135-6337insAGCTCCTGGGGAGGGC
XR_001748726.2:n.481+29_481+30insAGCTCCTGGGGAGGGC
XR_001748727.1:n.544+29_544+30insAGCTCCTGGGGAGGGC
XR_001748728.1:n.544+29_544+30insAGCTCCTGGGGAGGGC
XR_001748729.2:n.481+29_481+30insAGCTCCTGGGGAGGGC
XR_944559.2:n.534+29_534+30insAGCTCCTGGGGAGGGC
NM_001256796.2:c.475+29_475+30insAGCTCCTGGGGAGGGC	NP_001243725.1:n.475+29_475+30insAGCTCCTGGGGAGGGC
NM_001261397.2:c.427+29_427+30insAGCTCCTGGGGAGGGC	NP_001248326.1:n.427+29_427+30insAGCTCCTGGGGAGGGC
NM_001261398.2:c.427+29_427+30insAGCTCCTGGGGAGGGC	NP_001248327.1:n.427+29_427+30insAGCTCCTGGGGAGGGC
NM_002560.3:c.427+29_427+30insAGCTCCTGGGGAGGGC MANE Select	NP_002551.2:n.427+29_427+30insAGCTCCTGGGGAGGGC
NR_046372.2:n.463+29_463+30insAGCTCCTGGGGAGGGC
NR_046373.2:n.315+29_315+30insAGCTCCTGGGGAGGGC