Canonical Allele Identifier: CA2072975038

Gene: P2RX2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132621535G= , CM000674.2:g.132621535G=	GRCh38
NC_000012.11:g.133198121G= , CM000674.1:g.133198121G=	GRCh37
NC_000012.10:g.131708194G=	NCBI36
NG_033909.1:g.7756G=

Transcript Alleles

HGVS	Amino-acid Change
NM_170682.4:c.1057G= MANE Select	NP_733782.1:p.Gly353=
ENST00000643471.2:c.1057G= MANE Select	ENSP00000494644.1:p.Gly353=
NM_001282164.1:c.955G=	NP_001269093.1:p.Gly319=
NM_001282164.2:c.955G=	NP_001269093.1:p.Gly319=
NM_001282165.1:c.*26G=	NP_001269094.1:n.*26G=
NM_001282165.2:c.*26G=	NP_001269094.1:n.*26G=
NM_012226.4:c.841G=	NP_036358.2:p.Gly281=
NM_012226.5:c.841G=	NP_036358.2:p.Gly281=
NM_016318.3:c.985G=	NP_057402.1:p.Gly329=
NM_016318.4:c.985G=	NP_057402.1:p.Gly329=
NM_170682.3:c.1057G=	NP_733782.1:p.Gly353=
NM_170683.3:c.1057G=	NP_733783.1:p.Gly353=
NM_170683.4:c.1057G=	NP_733783.1:p.Gly353=
NM_174872.2:c.781G=	NP_777361.1:p.Gly261=
NM_174872.3:c.781G=	NP_777361.1:p.Gly261=
NM_174873.2:c.1057G=	NP_777362.1:p.Gly353=
NM_174873.3:c.1057G=	NP_777362.1:p.Gly353=
ENST00000343948.8:c.1057G=	ENSP00000343339.4:p.Gly353=
ENST00000348800.9:c.1057G=	ENSP00000345095.5:p.Gly353=
ENST00000350048.9:c.985G=	ENSP00000343904.5:p.Gly329=
ENST00000351222.8:c.781G=	ENSP00000344502.4:p.Gly261=
ENST00000352418.8:c.841G=	ENSP00000341419.4:p.Gly281=
ENST00000389110.7:c.1057G=	ENSP00000373762.3:p.Gly353=
ENST00000449132.6:c.955G=	ENSP00000405531.2:p.Gly319=
ENST00000542301.2:c.1076G=	ENSP00000444477.2:n.1076G=
XM_005266154.2:c.1180G=	XP_005266211.1:p.Gly394=
XM_005266154.4:c.1180G=	XP_005266211.1:p.Gly394=
XM_005266155.3:c.1057G=	XP_005266212.1:p.Gly353=
XM_005266155.5:c.1057G=	XP_005266212.1:p.Gly353=
XM_005266156.3:c.1057G=	XP_005266213.1:p.Gly353=
XM_005266156.5:c.1057G=	XP_005266213.1:p.Gly353=
XM_011534786.1:c.985G=	XP_011533088.1:p.Gly329=
XM_011534786.3:c.985G=	XP_011533088.1:p.Gly329=
XM_017019035.2:c.1057G=	XP_016874524.1:p.Gly353=