Canonical Allele Identifier: CA2621406502

Gene: P2RX4

Linked Data

• gnomAD v4: 12-121222226-G-GGCAAAACCC

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121222226_121222227insGCAAAACCC , CM000674.2:g.121222226_121222227insGCAAAACCC	GRCh38
NC_000012.11:g.121660029_121660030insGCAAAACCC , CM000674.1:g.121660029_121660030insGCAAAACCC	GRCh37
NC_000012.10:g.120144412_120144413insGCAAAACCC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337233.9:c.427+60_427+61insGCAAAACCC MANE Select	ENSP00000336607.4:n.427+60_427+61insGCAAAACCC
ENST00000314442.7:n.4561+60_4561+61insGCAAAACCC
ENST00000337233.8:c.427+60_427+61insGCAAAACCC	ENSP00000336607.4:n.427+60_427+61insGCAAAACCC
ENST00000359949.11:c.475+60_475+61insGCAAAACCC	ENSP00000353032.7:n.475+60_475+61insGCAAAACCC
ENST00000499638.6:n.523_524insGCAAAACCC
ENST00000538417.2:c.357+60_357+61insGCAAAACCC
ENST00000538701.5:c.135-6307_135-6306insGCAAAACCC	ENSP00000444033.1:n.135-6307_135-6306insGCAAAACCC
ENST00000540930.5:n.463+60_463+61insGCAAAACCC
ENST00000541187.5:n.273+60_273+61insGCAAAACCC
ENST00000542067.5:c.427+60_427+61insGCAAAACCC	ENSP00000438329.1:n.427+60_427+61insGCAAAACCC
ENST00000543171.5:c.427+60_427+61insGCAAAACCC	ENSP00000438131.2:n.427+60_427+61insGCAAAACCC
ENST00000543318.5:c.427+60_427+61insGCAAAACCC	ENSP00000444274.1:n.427+60_427+61insGCAAAACCC
ENST00000543430.5:n.475+60_475+61insGCAAAACCC
ENST00000543984.5:c.*120+60_*120+61insGCAAAACCC	ENSP00000439386.1:n.*120+60_*120+61insGCAAAACCC
NM_001256796.1:c.475+60_475+61insGCAAAACCC	NP_001243725.1:n.475+60_475+61insGCAAAACCC
NM_001261397.1:c.427+60_427+61insGCAAAACCC	NP_001248326.1:n.427+60_427+61insGCAAAACCC
NM_001261398.1:c.427+60_427+61insGCAAAACCC	NP_001248327.1:n.427+60_427+61insGCAAAACCC
NM_002560.2:c.427+60_427+61insGCAAAACCC	NP_002551.2:n.427+60_427+61insGCAAAACCC
NR_046372.1:n.731+60_731+61insGCAAAACCC
NR_046373.1:n.583+60_583+61insGCAAAACCC
XM_011538416.1:c.135-6307_135-6306insGCAAAACCC	XP_011536718.1:n.135-6307_135-6306insGCAAAACCC
XM_011538417.1:c.475+60_475+61insGCAAAACCC	XP_011536719.1:n.475+60_475+61insGCAAAACCC
XR_944559.1:n.535+60_535+61insGCAAAACCC
XM_011538416.2:c.135-6307_135-6306insGCAAAACCC	XP_011536718.1:n.135-6307_135-6306insGCAAAACCC
XR_001748726.2:n.481+60_481+61insGCAAAACCC
XR_001748727.1:n.544+60_544+61insGCAAAACCC
XR_001748728.1:n.544+60_544+61insGCAAAACCC
XR_001748729.2:n.481+60_481+61insGCAAAACCC
XR_944559.2:n.534+60_534+61insGCAAAACCC
NM_001256796.2:c.475+60_475+61insGCAAAACCC	NP_001243725.1:n.475+60_475+61insGCAAAACCC
NM_001261397.2:c.427+60_427+61insGCAAAACCC	NP_001248326.1:n.427+60_427+61insGCAAAACCC
NM_001261398.2:c.427+60_427+61insGCAAAACCC	NP_001248327.1:n.427+60_427+61insGCAAAACCC
NM_002560.3:c.427+60_427+61insGCAAAACCC MANE Select	NP_002551.2:n.427+60_427+61insGCAAAACCC
NR_046372.2:n.463+60_463+61insGCAAAACCC
NR_046373.2:n.315+60_315+61insGCAAAACCC