Canonical Allele Identifier: CA2603372394
Gene: P2RX7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.121132955_121132956insC , CM000674.2:g.121132955_121132956insC GRCh38
NC_000012.11:g.121570758_121570759insC , CM000674.1:g.121570758_121570759insC GRCh37
NC_000012.10:g.120055141_120055142insC NCBI36
NG_011471.2:g.5081_5082insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000328963.10:c.-16_-15insC MANE Select ENSP00000330696.6:n.-16_-15insC
ENST00000261826.10:c.-16_-15insC ENSP00000261826.6:n.-16_-15insC
ENST00000328963.9:c.-16_-15insC ENSP00000330696.6:n.-16_-15insC
ENST00000535928.5:c.-16_-15insC ENSP00000439961.1:n.-16_-15insC
ENST00000537312.5:c.-16_-15insC ENSP00000438586.1:n.-16_-15insC
ENST00000539695.5:n.54_55insC
ENST00000545434.5:c.-16_-15insC ENSP00000445564.1:n.-16_-15insC
NM_002562.5:c.-16_-15insC NP_002553.3:n.-16_-15insC
NR_033948.1:n.128_129insC
NR_033949.1:n.128_129insC
NR_033950.1:n.128_129insC
NR_033951.1:n.128_129insC
NR_033952.1:n.128_129insC
NR_033953.1:n.137_138insC
NR_033954.1:n.128_129insC
NR_033955.1:n.128_129insC
NR_033956.1:n.128_129insC
XM_011538418.1:c.-16_-15insC XP_011536720.1:n.-16_-15insC
XM_011538419.1:c.-159_-158insC XP_011536721.1:n.-159_-158insC
XM_011538419.3:c.-159_-158insC XP_011536721.1:n.-159_-158insC
XM_017019364.2:c.-529_-528insC XP_016874853.1:n.-529_-528insC
XM_017019365.2:c.-360_-359insC XP_016874854.1:n.-360_-359insC
XM_017019366.2:c.-696_-695insC XP_016874855.1:n.-696_-695insC
XM_017019367.2:c.-527_-526insC XP_016874856.1:n.-527_-526insC
XR_001749352.2:n.187-6115_187-6114insG
XR_001749354.2:n.187-6115_187-6114insG
NM_002562.6:c.-16_-15insC MANE Select NP_002553.3:n.-16_-15insC
NR_033948.2:n.80_81insC
NR_033949.2:n.80_81insC
NR_033950.2:n.80_81insC
NR_033951.2:n.80_81insC
NR_033952.2:n.80_81insC
NR_033953.2:n.80_81insC
NR_033954.2:n.80_81insC
NR_033955.2:n.80_81insC
NR_033956.2:n.80_81insC