Canonical Allele Identifier: CA2733071395
Gene: P2RX1 HGNC NCBI

Linked Data

dbSNP Id: rs2144084315

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.3914069_3914082del , CM000679.2:g.3914069_3914082del GRCh38
NC_000017.10:g.3817363_3817376del , CM000679.1:g.3817363_3817376del GRCh37
NC_000017.9:g.3764112_3764125del NCBI36
NG_012109.1:g.7591_7604del

Transcript Alleles

HGVS Amino-acid Change
ENST00000225538.4:c.137+2013_137+2026del MANE Select ENSP00000225538.3:n.137+2013_137+2026del
ENST00000225538.3:c.137+2013_137+2026del ENSP00000225538.3:n.137+2013_137+2026del
ENST00000571637.1:c.*596+1270_*596+1283del ENSP00000460449.1:n.*596+1270_*596+1283del
ENST00000572418.1:n.364+2013_364+2026del
NM_002558.3:c.137+2013_137+2026del NP_002549.1:n.137+2013_137+2026del
XM_006721529.1:c.137+2013_137+2026del XP_006721592.1:n.137+2013_137+2026del
XM_011523895.1:c.173+1310_173+1323del XP_011522197.1:n.173+1310_173+1323del
XM_011523896.1:c.173+1310_173+1323del XP_011522198.1:n.173+1310_173+1323del
XM_011523897.1:c.137+2013_137+2026del XP_011522199.1:n.137+2013_137+2026del
XM_011523898.1:c.173+1310_173+1323del XP_011522200.1:n.173+1310_173+1323del
XM_011523899.1:c.173+1310_173+1323del XP_011522201.1:n.173+1310_173+1323del
XM_011523900.1:c.173+1310_173+1323del XP_011522202.1:n.173+1310_173+1323del
XR_934028.1:n.1082+1310_1082+1323del
XR_934029.1:n.1082+1310_1082+1323del
XR_934030.1:n.1082+1310_1082+1323del
XM_006721529.2:c.137+2013_137+2026del XP_006721592.1:n.137+2013_137+2026del
XM_011523896.3:c.173+1310_173+1323del XP_011522198.1:n.173+1310_173+1323del
XM_011523897.2:c.137+2013_137+2026del XP_011522199.1:n.137+2013_137+2026del
XM_011523898.3:c.173+1310_173+1323del XP_011522200.1:n.173+1310_173+1323del
XM_011523899.3:c.173+1310_173+1323del XP_011522201.1:n.173+1310_173+1323del
XM_011523900.3:c.173+1310_173+1323del XP_011522202.1:n.173+1310_173+1323del
XR_934029.3:n.1116+1310_1116+1323del
XR_934030.3:n.1116+1310_1116+1323del
NM_002558.4:c.137+2013_137+2026del MANE Select NP_002549.1:n.137+2013_137+2026del