Canonical Allele Identifier: CA6891567

Gene: P2RX2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132620308_132620310del , CM000674.2:g.132620308_132620310del	GRCh38
NC_000012.11:g.133196894_133196896del , CM000674.1:g.133196894_133196896del	GRCh37
NC_000012.10:g.131706967_131706969del	NCBI36
NG_033909.1:g.6529_6531del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643471.2:c.596_598del MANE Select	ENSP00000494644.1:p.Ile199del
ENST00000343948.8:c.596_598del	ENSP00000343339.4:p.Ile199del
ENST00000348800.9:c.596_598del	ENSP00000345095.5:p.Ile199del
ENST00000350048.9:c.524_526del	ENSP00000343904.5:p.Ile175del
ENST00000351222.8:c.320_322del	ENSP00000344502.4:p.Ile107del
ENST00000352418.8:c.380_382del	ENSP00000341419.4:p.Ile127del
ENST00000389110.7:c.596_598del	ENSP00000373762.3:p.Ile199del
ENST00000449132.6:c.489_491del	ENSP00000405531.2:p.His163del
ENST00000542301.2:c.596_598del	ENSP00000444477.2:p.Ile199del
NM_001282164.1:c.489_491del	NP_001269093.1:p.His163del
NM_001282165.1:c.596_598del	NP_001269094.1:p.Ile199del
NM_012226.4:c.380_382del	NP_036358.2:p.Ile127del
NM_016318.3:c.524_526del	NP_057402.1:p.Ile175del
NM_170682.3:c.596_598del	NP_733782.1:p.Ile199del
NM_170683.3:c.596_598del	NP_733783.1:p.Ile199del
NM_174872.2:c.320_322del	NP_777361.1:p.Ile107del
NM_174873.2:c.596_598del	NP_777362.1:p.Ile199del
XM_005266154.2:c.596_598del	XP_005266211.1:p.Ile199del
XM_005266155.3:c.596_598del	XP_005266212.1:p.Ile199del
XM_005266156.3:c.596_598del	XP_005266213.1:p.Ile199del
XM_011534786.1:c.524_526del	XP_011533088.1:p.Ile175del
XM_005266154.4:c.596_598del	XP_005266211.1:p.Ile199del
XM_005266155.5:c.596_598del	XP_005266212.1:p.Ile199del
XM_005266156.5:c.596_598del	XP_005266213.1:p.Ile199del
XM_011534786.3:c.524_526del	XP_011533088.1:p.Ile175del
XM_017019035.2:c.596_598del	XP_016874524.1:p.Ile199del
NM_001282164.2:c.489_491del	NP_001269093.1:p.His163del
NM_001282165.2:c.596_598del	NP_001269094.1:p.Ile199del
NM_012226.5:c.380_382del	NP_036358.2:p.Ile127del
NM_016318.4:c.524_526del	NP_057402.1:p.Ile175del
NM_170682.4:c.596_598del MANE Select	NP_733782.1:p.Ile199del
NM_170683.4:c.596_598del	NP_733783.1:p.Ile199del
NM_174872.3:c.320_322del	NP_777361.1:p.Ile107del
NM_174873.3:c.596_598del	NP_777362.1:p.Ile199del