Canonical Allele Identifier: CA377642069

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058332C>G (hg19) ; chr10:g.94298575C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298575C>G , CM000672.2:g.94298575C>G	GRCh38
NC_000010.10:g.96058332C>G , CM000672.1:g.96058332C>G	GRCh37
NC_000010.9:g.96048322C>G	NCBI36
NG_015799.1:g.309587C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371375.2:c.4440C>G	ENSP00000360426.1:p.Tyr1480Ter
ENST00000685253.1:c.*1907C>G	ENSP00000509405.1:n.*1907C>G
ENST00000685889.1:n.2099C>G
ENST00000686807.1:n.783C>G
ENST00000686954.1:c.*648C>G	ENSP00000508416.1:n.*648C>G
ENST00000688810.1:c.4392C>G	ENSP00000509140.1:p.Tyr1464Ter
ENST00000689233.1:n.9572C>G
ENST00000690340.1:n.3037C>G
ENST00000692286.1:c.5232C>G	ENSP00000509490.1:p.Tyr1744Ter
ENST00000692396.1:c.5316C>G	ENSP00000508605.1:p.Tyr1772Ter
ENST00000371380.8:c.5364C>G MANE Select	ENSP00000360431.2:p.Tyr1788Ter
ENST00000371385.8:c.4338C>G	ENSP00000360438.4:p.Tyr1446Ter
ENST00000674738.1:c.3919C>G
ENST00000674827.1:c.3480C>G	ENSP00000502523.1:p.Tyr1160Ter
ENST00000675218.1:c.4440C>G	ENSP00000501910.1:p.Tyr1480Ter
ENST00000675487.1:c.*1297C>G	ENSP00000502340.1:n.*1297C>G
ENST00000675718.1:c.4633C>G
ENST00000260766.7:c.5364C>G	ENSP00000260766.3:p.Tyr1788Ter
ENST00000371375.1:c.4440C>G	ENSP00000360426.1:p.Tyr1480Ter
ENST00000371380.7:c.5364C>G	ENSP00000360431.2:p.Tyr1788Ter
ENST00000371385.7:c.4440C>G	ENSP00000360438.3:p.Tyr1480Ter
NM_001165979.2:c.4440C>G	NP_001159451.1:p.Tyr1480Ter
NM_001288989.1:c.5316C>G	NP_001275918.1:p.Tyr1772Ter
NM_016341.3:c.5364C>G	NP_057425.3:p.Tyr1788Ter
XM_006717885.2:c.5406C>G	XP_006717948.1:p.Tyr1802Ter
XM_006717886.2:c.5406C>G	XP_006717949.1:p.Tyr1802Ter
XM_006717888.2:c.5403C>G	XP_006717951.1:p.Tyr1801Ter
XM_006717889.2:c.5358C>G	XP_006717952.1:p.Tyr1786Ter
XM_006717890.1:c.4482C>G	XP_006717953.1:p.Tyr1494Ter
XM_011539849.1:c.5406C>G	XP_011538151.1:p.Tyr1802Ter
XM_011539850.1:c.4251C>G	XP_011538152.1:p.Tyr1417Ter
XM_006717885.4:c.5406C>G	XP_006717948.1:p.Tyr1802Ter
XM_006717888.4:c.5403C>G	XP_006717951.1:p.Tyr1801Ter
XM_006717889.4:c.5358C>G	XP_006717952.1:p.Tyr1786Ter
XM_006717890.3:c.4482C>G	XP_006717953.1:p.Tyr1494Ter
XM_011539849.3:c.5406C>G	XP_011538151.1:p.Tyr1802Ter
XM_011539850.3:c.4251C>G	XP_011538152.1:p.Tyr1417Ter
XM_017016310.2:c.5406C>G	XP_016871799.1:p.Tyr1802Ter
XM_017016311.2:c.5406C>G	XP_016871800.1:p.Tyr1802Ter
XM_017016312.2:c.4392C>G	XP_016871801.1:p.Tyr1464Ter
NM_001288989.2:c.5316C>G	NP_001275918.1:p.Tyr1772Ter
NM_016341.4:c.5364C>G MANE Select	NP_057425.3:p.Tyr1788Ter