Canonical Allele Identifier: CA2727233749

Gene: P2RX7

Linked Data

• dbSNP Id: rs2135958814

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121133111_121133112del , CM000674.2:g.121133111_121133112del	GRCh38
NC_000012.11:g.121570914_121570915del , CM000674.1:g.121570914_121570915del	GRCh37
NC_000012.10:g.120055297_120055298del	NCBI36
NG_011471.2:g.5237_5238del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328963.10:c.125+16_125+17del MANE Select	ENSP00000330696.6:n.125+16_125+17del
ENST00000261826.10:c.125+16_125+17del	ENSP00000261826.6:n.125+16_125+17del
ENST00000328963.9:c.125+16_125+17del	ENSP00000330696.6:n.125+16_125+17del
ENST00000535250.5:c.125+16_125+17del	ENSP00000442572.2:n.125+16_125+17del
ENST00000535600.2:c.125+16_125+17del	ENSP00000442470.1:n.125+16_125+17del
ENST00000535928.5:c.125+16_125+17del	ENSP00000439961.1:n.125+16_125+17del
ENST00000537312.5:c.125+16_125+17del	ENSP00000438586.1:n.125+16_125+17del
ENST00000538011.5:c.125+16_125+17del	ENSP00000439247.1:n.125+16_125+17del
ENST00000539606.5:c.125+16_125+17del	ENSP00000445325.1:n.125+16_125+17del
ENST00000539695.5:n.194+16_194+17del
ENST00000541022.5:c.125+16_125+17del	ENSP00000441230.1:n.125+16_125+17del
ENST00000541564.5:c.125+16_125+17del	ENSP00000443640.1:n.125+16_125+17del
ENST00000541716.5:c.125+16_125+17del	ENSP00000437729.1:n.125+16_125+17del
ENST00000545434.5:c.125+16_125+17del	ENSP00000445564.1:n.125+16_125+17del
NM_002562.5:c.125+16_125+17del	NP_002553.3:n.125+16_125+17del
NR_033948.1:n.268+16_268+17del
NR_033949.1:n.268+16_268+17del
NR_033950.1:n.268+16_268+17del
NR_033951.1:n.268+16_268+17del
NR_033952.1:n.268+16_268+17del
NR_033953.1:n.277+16_277+17del
NR_033954.1:n.268+16_268+17del
NR_033955.1:n.268+16_268+17del
NR_033956.1:n.268+16_268+17del
XM_011538418.1:c.125+16_125+17del	XP_011536720.1:n.125+16_125+17del
XM_011538419.1:c.-19+16_-19+17del	XP_011536721.1:n.-19+16_-19+17del
XM_011538420.1:c.-437+16_-437+17del	XP_011536722.1:n.-437+16_-437+17del
XM_011538419.3:c.-19+16_-19+17del	XP_011536721.1:n.-19+16_-19+17del
XM_011538420.3:c.-437+16_-437+17del	XP_011536722.1:n.-437+16_-437+17del
XM_017019364.2:c.-389+16_-389+17del	XP_016874853.1:n.-389+16_-389+17del
XM_017019365.2:c.-220+16_-220+17del	XP_016874854.1:n.-220+16_-220+17del
XM_017019366.2:c.-556+16_-556+17del	XP_016874855.1:n.-556+16_-556+17del
XM_017019367.2:c.-387+16_-387+17del	XP_016874856.1:n.-387+16_-387+17del
XR_001749352.2:n.187-6269_187-6268del
XR_001749354.2:n.187-6269_187-6268del
NM_002562.6:c.125+16_125+17del MANE Select	NP_002553.3:n.125+16_125+17del
NR_033948.2:n.220+16_220+17del
NR_033949.2:n.220+16_220+17del
NR_033950.2:n.220+16_220+17del
NR_033951.2:n.220+16_220+17del
NR_033952.2:n.220+16_220+17del
NR_033953.2:n.220+16_220+17del
NR_033954.2:n.220+16_220+17del
NR_033955.2:n.220+16_220+17del
NR_033956.2:n.220+16_220+17del