Canonical Allele Identifier: CA2621406205

Gene: P2RX4

Linked Data

• gnomAD v4: 12-121222160-AGCAACGGTACGAGCTTGTGGCC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121222161_121222182del , CM000674.2:g.121222161_121222182del	GRCh38
NC_000012.11:g.121659964_121659985del , CM000674.1:g.121659964_121659985del	GRCh37
NC_000012.10:g.120144347_120144368del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337233.9:c.422_427+16del
ENST00000314442.7:n.4556_4561+16del
ENST00000337233.8:c.422_427+16del
ENST00000359949.11:c.470_475+16del
ENST00000499638.6:n.458_479del
ENST00000538417.2:c.352_357+16del
ENST00000538701.5:c.135-6372_135-6351del	ENSP00000444033.1:n.135-6372_135-6351del
ENST00000540930.5:n.458_463+16del
ENST00000541187.5:n.268_273+16del
ENST00000542067.5:c.422_427+16del
ENST00000543171.5:c.422_427+16del
ENST00000543318.5:c.422_427+16del
ENST00000543430.5:n.470_475+16del
ENST00000543984.5:c.*115_*120+16del
NM_001256796.1:c.470_475+16del
NM_001261397.1:c.422_427+16del
NM_001261398.1:c.422_427+16del
NM_002560.2:c.422_427+16del
NR_046372.1:n.726_731+16del
NR_046373.1:n.578_583+16del
XM_011538416.1:c.135-6372_135-6351del	XP_011536718.1:n.135-6372_135-6351del
XM_011538417.1:c.470_475+16del
XR_944559.1:n.530_535+16del
XM_011538416.2:c.135-6372_135-6351del	XP_011536718.1:n.135-6372_135-6351del
XR_001748726.2:n.476_481+16del
XR_001748727.1:n.539_544+16del
XR_001748728.1:n.539_544+16del
XR_001748729.2:n.476_481+16del
XR_944559.2:n.529_534+16del
NM_001256796.2:c.470_475+16del
NM_001261397.2:c.422_427+16del
NM_001261398.2:c.422_427+16del
NM_002560.3:c.422_427+16del
NR_046372.2:n.458_463+16del
NR_046373.2:n.310_315+16del