Canonical Allele Identifier: CA6891897

Gene: P2RX2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132621888T>A , CM000674.2:g.132621888T>A	GRCh38
NC_000012.11:g.133198474T>A , CM000674.1:g.133198474T>A	GRCh37
NC_000012.10:g.131708547T>A	NCBI36
NG_033840.1:g.70637A>T , LRG_789:g.70637A>T
NG_033909.1:g.8109T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643471.2:c.1332T>A MANE Select	ENSP00000494644.1:p.Pro444=
ENST00000343948.8:c.1410T>A	ENSP00000343339.4:p.Pro470=
ENST00000348800.9:c.1141-10T>A	ENSP00000345095.5:n.1141-10T>A
ENST00000350048.9:c.1260T>A	ENSP00000343904.5:p.Pro420=
ENST00000351222.8:c.1056T>A	ENSP00000344502.4:p.Pro352=
ENST00000352418.8:c.1116T>A	ENSP00000341419.4:p.Pro372=
ENST00000389110.7:c.1332T>A	ENSP00000373762.3:p.Pro444=
ENST00000449132.6:c.1039-10T>A	ENSP00000405531.2:n.1039-10T>A
ENST00000542301.2:c.1429T>A	ENSP00000444477.2:n.1429T>A
NM_001282164.1:c.1039-10T>A	NP_001269093.1:n.1039-10T>A
NM_001282165.1:c.*379T>A	NP_001269094.1:n.*379T>A
NM_012226.4:c.1116T>A	NP_036358.2:p.Pro372=
NM_016318.3:c.1260T>A	NP_057402.1:p.Pro420=
NM_170682.3:c.1332T>A	NP_733782.1:p.Pro444=
NM_170683.3:c.1410T>A	NP_733783.1:p.Pro470=
NM_174872.2:c.1056T>A	NP_777361.1:p.Pro352=
NM_174873.2:c.1141-10T>A	NP_777362.1:n.1141-10T>A
XM_005266154.2:c.1455T>A	XP_005266211.1:p.Pro485=
XM_005266155.3:c.1219-112T>A	XP_005266212.1:n.1219-112T>A
XM_005266156.3:c.1219-10T>A	XP_005266213.1:n.1219-10T>A
XM_011534786.1:c.1338T>A	XP_011533088.1:p.Pro446=
XM_005266154.4:c.1455T>A	XP_005266211.1:p.Pro485=
XM_005266155.5:c.1219-112T>A	XP_005266212.1:n.1219-112T>A
XM_005266156.5:c.1219-10T>A	XP_005266213.1:n.1219-10T>A
XM_011534786.3:c.1338T>A	XP_011533088.1:p.Pro446=
XM_017019035.2:c.1141-112T>A	XP_016874524.1:n.1141-112T>A
NM_001282164.2:c.1039-10T>A	NP_001269093.1:n.1039-10T>A
NM_001282165.2:c.*379T>A	NP_001269094.1:n.*379T>A
NM_012226.5:c.1116T>A	NP_036358.2:p.Pro372=
NM_016318.4:c.1260T>A	NP_057402.1:p.Pro420=
NM_170682.4:c.1332T>A MANE Select	NP_733782.1:p.Pro444=
NM_170683.4:c.1410T>A	NP_733783.1:p.Pro470=
NM_174872.3:c.1056T>A	NP_777361.1:p.Pro352=
NM_174873.3:c.1141-10T>A	NP_777362.1:n.1141-10T>A