Canonical Allele Identifier: CA2797733423

Gene: P2RX4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121221962_121221963insAACACACCC , CM000674.2:g.121221962_121221963insAACACACCC	GRCh38
NC_000012.11:g.121659765_121659766insAACACACCC , CM000674.1:g.121659765_121659766insAACACACCC	GRCh37
NC_000012.10:g.120144148_120144149insAACACACCC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337233.9:c.332_333insAACACACCC MANE Select	ENSP00000336607.4:p.Gln111_Thr112insThrHisPro
ENST00000314442.7:n.4466_4467insAACACACCC
ENST00000337233.8:c.332_333insAACACACCC	ENSP00000336607.4:p.Gln111_Thr112insThrHisPro
ENST00000359949.11:c.380_381insAACACACCC	ENSP00000353032.7:p.Gln127_Thr128insThrHisPro
ENST00000499638.6:n.368_369insAACACACCC
ENST00000538417.2:c.262_263insAACACACCC
ENST00000538701.5:c.135-6571_135-6570insAACACACCC	ENSP00000444033.1:n.135-6571_135-6570insAACACACCC
ENST00000540930.5:n.368_369insAACACACCC
ENST00000541187.5:n.178_179insAACACACCC
ENST00000542067.5:c.332_333insAACACACCC	ENSP00000438329.1:p.Gln111_Thr112insThrHisPro
ENST00000543171.5:c.332_333insAACACACCC	ENSP00000438131.2:p.Gln111_Thr112insThrHisPro
ENST00000543318.5:c.332_333insAACACACCC	ENSP00000444274.1:p.Gln111_Thr112insThrHisPro
ENST00000543430.5:n.380_381insAACACACCC
ENST00000543984.5:c.*25_*26insAACACACCC	ENSP00000439386.1:n.*25_*26insAACACACCC
NM_001256796.1:c.380_381insAACACACCC	NP_001243725.1:p.Gln127_Thr128insThrHisPro
NM_001261397.1:c.332_333insAACACACCC	NP_001248326.1:p.Gln111_Thr112insThrHisPro
NM_001261398.1:c.332_333insAACACACCC	NP_001248327.1:p.Gln111_Thr112insThrHisPro
NM_002560.2:c.332_333insAACACACCC	NP_002551.2:p.Gln111_Thr112insThrHisPro
NR_046372.1:n.636_637insAACACACCC
NR_046373.1:n.488_489insAACACACCC
XM_011538416.1:c.135-6571_135-6570insAACACACCC	XP_011536718.1:n.135-6571_135-6570insAACACACCC
XM_011538417.1:c.380_381insAACACACCC	XP_011536719.1:p.Gln127_Thr128insThrHisPro
XR_944559.1:n.440_441insAACACACCC
XM_011538416.2:c.135-6571_135-6570insAACACACCC	XP_011536718.1:n.135-6571_135-6570insAACACACCC
XR_001748726.2:n.386_387insAACACACCC
XR_001748727.1:n.449_450insAACACACCC
XR_001748728.1:n.449_450insAACACACCC
XR_001748729.2:n.386_387insAACACACCC
XR_944559.2:n.439_440insAACACACCC
NM_001256796.2:c.380_381insAACACACCC	NP_001243725.1:p.Gln127_Thr128insThrHisPro
NM_001261397.2:c.332_333insAACACACCC	NP_001248326.1:p.Gln111_Thr112insThrHisPro
NM_001261398.2:c.332_333insAACACACCC	NP_001248327.1:p.Gln111_Thr112insThrHisPro
NM_002560.3:c.332_333insAACACACCC MANE Select	NP_002551.2:p.Gln111_Thr112insThrHisPro
NR_046372.2:n.368_369insAACACACCC
NR_046373.2:n.220_221insAACACACCC