Canonical Allele Identifier: CA377641892

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058249A>T (hg19) ; chr10:g.94298492A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298492A>T , CM000672.2:g.94298492A>T	GRCh38
NC_000010.10:g.96058249A>T , CM000672.1:g.96058249A>T	GRCh37
NC_000010.9:g.96048239A>T	NCBI36
NG_015799.1:g.309504A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4357A>T	ENSP00000360426.1:p.Asn1453Tyr
ENST00000685253.1:c.*1824A>T	ENSP00000509405.1:n.*1824A>T
ENST00000685889.1:n.2016A>T
ENST00000686807.1:n.700A>T
ENST00000686954.1:c.*565A>T	ENSP00000508416.1:n.*565A>T
ENST00000688810.1:c.4309A>T	ENSP00000509140.1:p.Asn1437Tyr
ENST00000689233.1:n.9489A>T
ENST00000690340.1:n.2954A>T
ENST00000692286.1:c.5149A>T	ENSP00000509490.1:p.Asn1717Tyr
ENST00000692396.1:c.5233A>T	ENSP00000508605.1:p.Asn1745Tyr
ENST00000371380.8:c.5281A>T MANE Select	ENSP00000360431.2:p.Asn1761Tyr
ENST00000371385.8:c.4255A>T	ENSP00000360438.4:p.Asn1419Tyr
ENST00000674738.1:c.3836A>T
ENST00000674827.1:c.3397A>T	ENSP00000502523.1:p.Asn1133Tyr
ENST00000675218.1:c.4357A>T	ENSP00000501910.1:p.Asn1453Tyr
ENST00000675487.1:c.*1214A>T	ENSP00000502340.1:n.*1214A>T
ENST00000675718.1:c.4550A>T
ENST00000260766.7:c.5281A>T	ENSP00000260766.3:p.Asn1761Tyr
ENST00000371375.1:c.4357A>T	ENSP00000360426.1:p.Asn1453Tyr
ENST00000371380.7:c.5281A>T	ENSP00000360431.2:p.Asn1761Tyr
ENST00000371385.7:c.4357A>T	ENSP00000360438.3:p.Asn1453Tyr
NM_001165979.2:c.4357A>T	NP_001159451.1:p.Asn1453Tyr
NM_001288989.1:c.5233A>T	NP_001275918.1:p.Asn1745Tyr
NM_016341.3:c.5281A>T	NP_057425.3:p.Asn1761Tyr
XM_006717885.2:c.5323A>T	XP_006717948.1:p.Asn1775Tyr
XM_006717886.2:c.5323A>T	XP_006717949.1:p.Asn1775Tyr
XM_006717888.2:c.5320A>T	XP_006717951.1:p.Asn1774Tyr
XM_006717889.2:c.5275A>T	XP_006717952.1:p.Asn1759Tyr
XM_006717890.1:c.4399A>T	XP_006717953.1:p.Asn1467Tyr
XM_011539849.1:c.5323A>T	XP_011538151.1:p.Asn1775Tyr
XM_011539850.1:c.4168A>T	XP_011538152.1:p.Asn1390Tyr
XM_006717885.4:c.5323A>T	XP_006717948.1:p.Asn1775Tyr
XM_006717888.4:c.5320A>T	XP_006717951.1:p.Asn1774Tyr
XM_006717889.4:c.5275A>T	XP_006717952.1:p.Asn1759Tyr
XM_006717890.3:c.4399A>T	XP_006717953.1:p.Asn1467Tyr
XM_011539849.3:c.5323A>T	XP_011538151.1:p.Asn1775Tyr
XM_011539850.3:c.4168A>T	XP_011538152.1:p.Asn1390Tyr
XM_017016310.2:c.5323A>T	XP_016871799.1:p.Asn1775Tyr
XM_017016311.2:c.5323A>T	XP_016871800.1:p.Asn1775Tyr
XM_017016312.2:c.4309A>T	XP_016871801.1:p.Asn1437Tyr
NM_001288989.2:c.5233A>T	NP_001275918.1:p.Asn1745Tyr
NM_016341.4:c.5281A>T MANE Select	NP_057425.3:p.Asn1761Tyr