Canonical Allele Identifier: CA2067739661
Gene: P2RX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.121222040_121222042delinsCCT , CM000674.2:g.121222040_121222042delinsCCT GRCh38
NC_000012.11:g.121659843_121659845delinsCCT , CM000674.1:g.121659843_121659845delinsCCT GRCh37
NC_000012.10:g.120144226_120144228delinsCCT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000337233.9:c.355-54_355-52delinsCCT MANE Select ENSP00000336607.4:n.355-54_355-52delinsCC...
ENST00000314442.7:n.4489-54_4489-52delinsCCT
ENST00000337233.8:c.355-54_355-52delinsCCT ENSP00000336607.4:n.355-54_355-52delinsCC...
ENST00000359949.11:c.403-54_403-52delinsCCT ENSP00000353032.7:n.403-54_403-52delinsCC...
ENST00000499638.6:n.391-54_391-52delinsCCT
ENST00000538417.2:c.285-54_285-52delinsCCT
ENST00000538701.5:c.135-6493_135-6491delinsCCT ENSP00000444033.1:n.135-6493_135-6491deli...
ENST00000540930.5:n.391-54_391-52delinsCCT
ENST00000541187.5:n.201-54_201-52delinsCCT
ENST00000542067.5:c.355-54_355-52delinsCCT ENSP00000438329.1:n.355-54_355-52delinsCC...
ENST00000543171.5:c.355-54_355-52delinsCCT ENSP00000438131.2:n.355-54_355-52delinsCC...
ENST00000543318.5:c.355-54_355-52delinsCCT ENSP00000444274.1:n.355-54_355-52delinsCC...
ENST00000543430.5:n.403-54_403-52delinsCCT
ENST00000543984.5:c.*48-54_*48-52delinsCCT ENSP00000439386.1:n.*48-54_*48-52delinsCC...
NM_001256796.1:c.403-54_403-52delinsCCT NP_001243725.1:n.403-54_403-52delinsCCT
NM_001261397.1:c.355-54_355-52delinsCCT NP_001248326.1:n.355-54_355-52delinsCCT
NM_001261398.1:c.355-54_355-52delinsCCT NP_001248327.1:n.355-54_355-52delinsCCT
NM_002560.2:c.355-54_355-52delinsCCT NP_002551.2:n.355-54_355-52delinsCCT
NR_046372.1:n.659-54_659-52delinsCCT
NR_046373.1:n.511-54_511-52delinsCCT
XM_011538416.1:c.135-6493_135-6491delinsCCT XP_011536718.1:n.135-6493_135-6491delinsC...
XM_011538417.1:c.403-54_403-52delinsCCT XP_011536719.1:n.403-54_403-52delinsCCT
XR_944559.1:n.463-54_463-52delinsCCT
XM_011538416.2:c.135-6493_135-6491delinsCCT XP_011536718.1:n.135-6493_135-6491delinsC...
XR_001748726.2:n.409-54_409-52delinsCCT
XR_001748727.1:n.472-54_472-52delinsCCT
XR_001748728.1:n.472-54_472-52delinsCCT
XR_001748729.2:n.409-54_409-52delinsCCT
XR_944559.2:n.462-54_462-52delinsCCT
NM_001256796.2:c.403-54_403-52delinsCCT NP_001243725.1:n.403-54_403-52delinsCCT
NM_001261397.2:c.355-54_355-52delinsCCT NP_001248326.1:n.355-54_355-52delinsCCT
NM_001261398.2:c.355-54_355-52delinsCCT NP_001248327.1:n.355-54_355-52delinsCCT
NM_002560.3:c.355-54_355-52delinsCCT MANE Select NP_002551.2:n.355-54_355-52delinsCCT
NR_046372.2:n.391-54_391-52delinsCCT
NR_046373.2:n.243-54_243-52delinsCCT