Canonical Allele Identifier: CA2067768432

Gene: P2RX7

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121132953G= , CM000674.2:g.121132953G=	GRCh38
NC_000012.11:g.121570756G= , CM000674.1:g.121570756G=	GRCh37
NC_000012.10:g.120055139G=	NCBI36
NG_011471.2:g.5079G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328963.10:c.-18G= MANE Select	ENSP00000330696.6:n.-18G=
ENST00000261826.10:c.-18G=	ENSP00000261826.6:n.-18G=
ENST00000328963.9:c.-18G=	ENSP00000330696.6:n.-18G=
ENST00000535928.5:c.-18G=	ENSP00000439961.1:n.-18G=
ENST00000537312.5:c.-18G=	ENSP00000438586.1:n.-18G=
ENST00000539695.5:n.52G=
ENST00000545434.5:c.-18G=	ENSP00000445564.1:n.-18G=
NM_002562.5:c.-18G=	NP_002553.3:n.-18G=
NR_033948.1:n.126G=
NR_033949.1:n.126G=
NR_033950.1:n.126G=
NR_033951.1:n.126G=
NR_033952.1:n.126G=
NR_033953.1:n.135G=
NR_033954.1:n.126G=
NR_033955.1:n.126G=
NR_033956.1:n.126G=
XM_011538418.1:c.-18G=	XP_011536720.1:n.-18G=
XM_011538419.1:c.-161G=	XP_011536721.1:n.-161G=
XM_011538419.3:c.-161G=	XP_011536721.1:n.-161G=
XM_017019364.2:c.-531G=	XP_016874853.1:n.-531G=
XM_017019365.2:c.-362G=	XP_016874854.1:n.-362G=
XM_017019366.2:c.-698G=	XP_016874855.1:n.-698G=
XM_017019367.2:c.-529G=	XP_016874856.1:n.-529G=
XR_001749352.2:n.187-6112C=
XR_001749354.2:n.187-6112C=
NM_002562.6:c.-18G= MANE Select	NP_002553.3:n.-18G=
NR_033948.2:n.78G=
NR_033949.2:n.78G=
NR_033950.2:n.78G=
NR_033951.2:n.78G=
NR_033952.2:n.78G=
NR_033953.2:n.78G=
NR_033954.2:n.78G=
NR_033955.2:n.78G=
NR_033956.2:n.78G=