Canonical Allele Identifier: CA6891345

Gene: P2RX2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132619017_132619030del , CM000674.2:g.132619017_132619030del	GRCh38
NC_000012.11:g.133195603_133195616del , CM000674.1:g.133195603_133195616del	GRCh37
NC_000012.10:g.131705676_131705689del	NCBI36
NG_033909.1:g.5238_5251del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643471.2:c.173+28_173+41del MANE Select	ENSP00000494644.1:n.173+28_173+41del
ENST00000343948.8:c.173+28_173+41del	ENSP00000343339.4:n.173+28_173+41del
ENST00000348800.9:c.173+28_173+41del	ENSP00000345095.5:n.173+28_173+41del
ENST00000350048.9:c.173+28_173+41del	ENSP00000343904.5:n.173+28_173+41del
ENST00000351222.8:c.105+96_105+109del	ENSP00000344502.4:n.105+96_105+109del
ENST00000352418.8:c.105+96_105+109del	ENSP00000341419.4:n.105+96_105+109del
ENST00000389110.7:c.173+28_173+41del	ENSP00000373762.3:n.173+28_173+41del
ENST00000449132.6:c.173+28_173+41del	ENSP00000405531.2:n.173+28_173+41del
ENST00000542301.2:c.173+28_173+41del	ENSP00000444477.2:n.173+28_173+41del
NM_001282164.1:c.173+28_173+41del	NP_001269093.1:n.173+28_173+41del
NM_001282165.1:c.173+28_173+41del	NP_001269094.1:n.173+28_173+41del
NM_012226.4:c.105+96_105+109del	NP_036358.2:n.105+96_105+109del
NM_016318.3:c.173+28_173+41del	NP_057402.1:n.173+28_173+41del
NM_170682.3:c.173+28_173+41del	NP_733782.1:n.173+28_173+41del
NM_170683.3:c.173+28_173+41del	NP_733783.1:n.173+28_173+41del
NM_174872.2:c.105+96_105+109del	NP_777361.1:n.105+96_105+109del
NM_174873.2:c.173+28_173+41del	NP_777362.1:n.173+28_173+41del
XM_005266154.2:c.173+28_173+41del	XP_005266211.1:n.173+28_173+41del
XM_005266155.3:c.173+28_173+41del	XP_005266212.1:n.173+28_173+41del
XM_005266156.3:c.173+28_173+41del	XP_005266213.1:n.173+28_173+41del
XM_011534786.1:c.173+28_173+41del	XP_011533088.1:n.173+28_173+41del
XM_005266154.4:c.173+28_173+41del	XP_005266211.1:n.173+28_173+41del
XM_005266155.5:c.173+28_173+41del	XP_005266212.1:n.173+28_173+41del
XM_005266156.5:c.173+28_173+41del	XP_005266213.1:n.173+28_173+41del
XM_011534786.3:c.173+28_173+41del	XP_011533088.1:n.173+28_173+41del
XM_017019035.2:c.173+28_173+41del	XP_016874524.1:n.173+28_173+41del
NM_001282164.2:c.173+28_173+41del	NP_001269093.1:n.173+28_173+41del
NM_001282165.2:c.173+28_173+41del	NP_001269094.1:n.173+28_173+41del
NM_012226.5:c.105+96_105+109del	NP_036358.2:n.105+96_105+109del
NM_016318.4:c.173+28_173+41del	NP_057402.1:n.173+28_173+41del
NM_170682.4:c.173+28_173+41del MANE Select	NP_733782.1:n.173+28_173+41del
NM_170683.4:c.173+28_173+41del	NP_733783.1:n.173+28_173+41del
NM_174872.3:c.105+96_105+109del	NP_777361.1:n.105+96_105+109del
NM_174873.3:c.173+28_173+41del	NP_777362.1:n.173+28_173+41del