Canonical Allele Identifier: CA2067739762

Gene: P2RX4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121222084_121222085delinsCT , CM000674.2:g.121222084_121222085delinsCT	GRCh38
NC_000012.11:g.121659887_121659888delinsCT , CM000674.1:g.121659887_121659888delinsCT	GRCh37
NC_000012.10:g.120144270_120144271delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337233.9:c.355-10_355-9delinsCT MANE Select	ENSP00000336607.4:n.355-10_355-9delinsCT
ENST00000314442.7:n.4489-10_4489-9delinsCT
ENST00000337233.8:c.355-10_355-9delinsCT	ENSP00000336607.4:n.355-10_355-9delinsCT
ENST00000359949.11:c.403-10_403-9delinsCT	ENSP00000353032.7:n.403-10_403-9delinsCT
ENST00000499638.6:n.391-10_391-9delinsCT
ENST00000538417.2:c.285-10_285-9delinsCT
ENST00000538701.5:c.135-6449_135-6448delinsCT	ENSP00000444033.1:n.135-6449_135-6448delinsCT
ENST00000540930.5:n.391-10_391-9delinsCT
ENST00000541187.5:n.201-10_201-9delinsCT
ENST00000542067.5:c.355-10_355-9delinsCT	ENSP00000438329.1:n.355-10_355-9delinsCT
ENST00000543171.5:c.355-10_355-9delinsCT	ENSP00000438131.2:n.355-10_355-9delinsCT
ENST00000543318.5:c.355-10_355-9delinsCT	ENSP00000444274.1:n.355-10_355-9delinsCT
ENST00000543430.5:n.403-10_403-9delinsCT
ENST00000543984.5:c.*48-10_*48-9delinsCT	ENSP00000439386.1:n.*48-10_*48-9delinsCT
NM_001256796.1:c.403-10_403-9delinsCT	NP_001243725.1:n.403-10_403-9delinsCT
NM_001261397.1:c.355-10_355-9delinsCT	NP_001248326.1:n.355-10_355-9delinsCT
NM_001261398.1:c.355-10_355-9delinsCT	NP_001248327.1:n.355-10_355-9delinsCT
NM_002560.2:c.355-10_355-9delinsCT	NP_002551.2:n.355-10_355-9delinsCT
NR_046372.1:n.659-10_659-9delinsCT
NR_046373.1:n.511-10_511-9delinsCT
XM_011538416.1:c.135-6449_135-6448delinsCT	XP_011536718.1:n.135-6449_135-6448delinsCT
XM_011538417.1:c.403-10_403-9delinsCT	XP_011536719.1:n.403-10_403-9delinsCT
XR_944559.1:n.463-10_463-9delinsCT
XM_011538416.2:c.135-6449_135-6448delinsCT	XP_011536718.1:n.135-6449_135-6448delinsCT
XR_001748726.2:n.409-10_409-9delinsCT
XR_001748727.1:n.472-10_472-9delinsCT
XR_001748728.1:n.472-10_472-9delinsCT
XR_001748729.2:n.409-10_409-9delinsCT
XR_944559.2:n.462-10_462-9delinsCT
NM_001256796.2:c.403-10_403-9delinsCT	NP_001243725.1:n.403-10_403-9delinsCT
NM_001261397.2:c.355-10_355-9delinsCT	NP_001248326.1:n.355-10_355-9delinsCT
NM_001261398.2:c.355-10_355-9delinsCT	NP_001248327.1:n.355-10_355-9delinsCT
NM_002560.3:c.355-10_355-9delinsCT MANE Select	NP_002551.2:n.355-10_355-9delinsCT
NR_046372.2:n.391-10_391-9delinsCT
NR_046373.2:n.243-10_243-9delinsCT