Canonical Allele Identifier: CA377642133

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058363C>A (hg19) ; chr10:g.94298606C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298606C>A , CM000672.2:g.94298606C>A	GRCh38
NC_000010.10:g.96058363C>A , CM000672.1:g.96058363C>A	GRCh37
NC_000010.9:g.96048353C>A	NCBI36
NG_015799.1:g.309618C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4471C>A	ENSP00000360426.1:p.Pro1491Thr
ENST00000685253.1:c.*1938C>A	ENSP00000509405.1:n.*1938C>A
ENST00000685889.1:n.2130C>A
ENST00000686807.1:n.814C>A
ENST00000686954.1:c.*679C>A	ENSP00000508416.1:n.*679C>A
ENST00000688810.1:c.4423C>A	ENSP00000509140.1:p.Pro1475Thr
ENST00000689233.1:n.9603C>A
ENST00000690340.1:n.3068C>A
ENST00000692286.1:c.5263C>A	ENSP00000509490.1:p.Pro1755Thr
ENST00000692396.1:c.5347C>A	ENSP00000508605.1:p.Pro1783Thr
ENST00000371380.8:c.5395C>A MANE Select	ENSP00000360431.2:p.Pro1799Thr
ENST00000371385.8:c.4369C>A	ENSP00000360438.4:p.Pro1457Thr
ENST00000674738.1:c.3950C>A
ENST00000674827.1:c.3511C>A	ENSP00000502523.1:p.Pro1171Thr
ENST00000675218.1:c.4471C>A	ENSP00000501910.1:p.Pro1491Thr
ENST00000675487.1:c.*1328C>A	ENSP00000502340.1:n.*1328C>A
ENST00000675718.1:c.4664C>A
ENST00000260766.7:c.5395C>A	ENSP00000260766.3:p.Pro1799Thr
ENST00000371375.1:c.4471C>A	ENSP00000360426.1:p.Pro1491Thr
ENST00000371380.7:c.5395C>A	ENSP00000360431.2:p.Pro1799Thr
ENST00000371385.7:c.4471C>A	ENSP00000360438.3:p.Pro1491Thr
NM_001165979.2:c.4471C>A	NP_001159451.1:p.Pro1491Thr
NM_001288989.1:c.5347C>A	NP_001275918.1:p.Pro1783Thr
NM_016341.3:c.5395C>A	NP_057425.3:p.Pro1799Thr
XM_006717885.2:c.5437C>A	XP_006717948.1:p.Pro1813Thr
XM_006717886.2:c.5437C>A	XP_006717949.1:p.Pro1813Thr
XM_006717888.2:c.5434C>A	XP_006717951.1:p.Pro1812Thr
XM_006717889.2:c.5389C>A	XP_006717952.1:p.Pro1797Thr
XM_006717890.1:c.4513C>A	XP_006717953.1:p.Pro1505Thr
XM_011539849.1:c.5437C>A	XP_011538151.1:p.Pro1813Thr
XM_011539850.1:c.4282C>A	XP_011538152.1:p.Pro1428Thr
XM_006717885.4:c.5437C>A	XP_006717948.1:p.Pro1813Thr
XM_006717888.4:c.5434C>A	XP_006717951.1:p.Pro1812Thr
XM_006717889.4:c.5389C>A	XP_006717952.1:p.Pro1797Thr
XM_006717890.3:c.4513C>A	XP_006717953.1:p.Pro1505Thr
XM_011539849.3:c.5437C>A	XP_011538151.1:p.Pro1813Thr
XM_011539850.3:c.4282C>A	XP_011538152.1:p.Pro1428Thr
XM_017016310.2:c.5437C>A	XP_016871799.1:p.Pro1813Thr
XM_017016311.2:c.5437C>A	XP_016871800.1:p.Pro1813Thr
XM_017016312.2:c.4423C>A	XP_016871801.1:p.Pro1475Thr
NM_001288989.2:c.5347C>A	NP_001275918.1:p.Pro1783Thr
NM_016341.4:c.5395C>A MANE Select	NP_057425.3:p.Pro1799Thr