Canonical Allele Identifier: CA386959201

Gene: P2RX7

Linked Data

• MyVariant Identifiers: chr12:g.121615140G>C (hg19) ; chr12:g.121177337G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121177337G>C , CM000674.2:g.121177337G>C	GRCh38
NC_000012.11:g.121615140G>C , CM000674.1:g.121615140G>C	GRCh37
NC_000012.10:g.120099523G>C	NCBI36
NG_011471.2:g.49463G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328963.10:c.1079G>C MANE Select	ENSP00000330696.6:p.Ser360Thr
ENST00000261826.10:c.*532G>C	ENSP00000261826.6:n.*532G>C
ENST00000328963.9:c.1079G>C	ENSP00000330696.6:p.Ser360Thr
ENST00000535250.5:c.1163G>C	ENSP00000442572.2:n.1163G>C
ENST00000535600.2:c.896G>C	ENSP00000442470.1:n.896G>C
ENST00000537312.5:c.*850G>C	ENSP00000438586.1:n.*850G>C
ENST00000538011.5:c.1218G>C	ENSP00000439247.1:n.1218G>C
ENST00000539606.5:c.1302G>C	ENSP00000445325.1:n.1302G>C
ENST00000539695.5:n.1248G>C
ENST00000541022.5:c.869G>C	ENSP00000441230.1:n.869G>C
ENST00000541564.5:c.942G>C	ENSP00000443640.1:n.942G>C
ENST00000541716.5:c.1090G>C	ENSP00000437729.1:n.1090G>C
NM_002562.5:c.1079G>C	NP_002553.3:p.Ser360Thr
NR_033948.1:n.1445G>C
NR_033949.1:n.1361G>C
NR_033950.1:n.1322G>C
NR_033951.1:n.1306G>C
NR_033952.1:n.1233G>C
NR_033953.1:n.1146G>C
NR_033954.1:n.1125G>C
NR_033955.1:n.1085G>C
NR_033956.1:n.1012G>C
XM_011538418.1:c.812G>C	XP_011536720.1:p.Ser271Thr
XM_011538419.1:c.767G>C	XP_011536721.1:p.Ser256Thr
XM_011538420.1:c.212G>C	XP_011536722.1:p.Ser71Thr
XR_945459.1:n.190-14920C>G
XR_945460.1:n.299-14920C>G
XM_011538419.3:c.767G>C	XP_011536721.1:p.Ser256Thr
XM_011538420.3:c.212G>C	XP_011536722.1:p.Ser71Thr
XM_017019364.2:c.719G>C	XP_016874853.1:p.Ser240Thr
XM_017019365.2:c.719G>C	XP_016874854.1:p.Ser240Thr
XM_017019366.2:c.326G>C	XP_016874855.1:p.Ser109Thr
XM_017019367.2:c.326G>C	XP_016874856.1:p.Ser109Thr
XR_001749352.2:n.186+26161C>G
XR_001749353.2:n.304-14920C>G
XR_001749354.2:n.186+26161C>G
XR_945459.3:n.187-14920C>G
XR_945460.3:n.299-14920C>G
NM_002562.6:c.1079G>C MANE Select	NP_002553.3:p.Ser360Thr
NR_033948.2:n.1397G>C
NR_033949.2:n.1313G>C
NR_033950.2:n.1274G>C
NR_033951.2:n.1258G>C
NR_033952.2:n.1185G>C
NR_033953.2:n.1089G>C
NR_033954.2:n.1077G>C
NR_033955.2:n.1037G>C
NR_033956.2:n.964G>C