Canonical Allele Identifier: CA470986507

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058257T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298500T>C , CM000672.2:g.94298500T>C	GRCh38
NC_000010.10:g.96058257T>C , CM000672.1:g.96058257T>C	GRCh37
NC_000010.9:g.96048247T>C	NCBI36
NG_015799.1:g.309512T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4365T>C	ENSP00000360426.1:p.Asn1455=
ENST00000685253.1:c.*1832T>C	ENSP00000509405.1:n.*1832T>C
ENST00000685889.1:n.2024T>C
ENST00000686807.1:n.708T>C
ENST00000686954.1:c.*573T>C	ENSP00000508416.1:n.*573T>C
ENST00000688810.1:c.4317T>C	ENSP00000509140.1:p.Asn1439=
ENST00000689233.1:n.9497T>C
ENST00000690340.1:n.2962T>C
ENST00000692286.1:c.5157T>C	ENSP00000509490.1:p.Asn1719=
ENST00000692396.1:c.5241T>C	ENSP00000508605.1:p.Asn1747=
ENST00000371380.8:c.5289T>C MANE Select	ENSP00000360431.2:p.Asn1763=
ENST00000371385.8:c.4263T>C	ENSP00000360438.4:p.Asn1421=
ENST00000674738.1:c.3844T>C
ENST00000674827.1:c.3405T>C	ENSP00000502523.1:p.Asn1135=
ENST00000675218.1:c.4365T>C	ENSP00000501910.1:p.Asn1455=
ENST00000675487.1:c.*1222T>C	ENSP00000502340.1:n.*1222T>C
ENST00000675718.1:c.4558T>C
ENST00000260766.7:c.5289T>C	ENSP00000260766.3:p.Asn1763=
ENST00000371375.1:c.4365T>C	ENSP00000360426.1:p.Asn1455=
ENST00000371380.7:c.5289T>C	ENSP00000360431.2:p.Asn1763=
ENST00000371385.7:c.4365T>C	ENSP00000360438.3:p.Asn1455=
NM_001165979.2:c.4365T>C	NP_001159451.1:p.Asn1455=
NM_001288989.1:c.5241T>C	NP_001275918.1:p.Asn1747=
NM_016341.3:c.5289T>C	NP_057425.3:p.Asn1763=
XM_006717885.2:c.5331T>C	XP_006717948.1:p.Asn1777=
XM_006717886.2:c.5331T>C	XP_006717949.1:p.Asn1777=
XM_006717888.2:c.5328T>C	XP_006717951.1:p.Asn1776=
XM_006717889.2:c.5283T>C	XP_006717952.1:p.Asn1761=
XM_006717890.1:c.4407T>C	XP_006717953.1:p.Asn1469=
XM_011539849.1:c.5331T>C	XP_011538151.1:p.Asn1777=
XM_011539850.1:c.4176T>C	XP_011538152.1:p.Asn1392=
XM_006717885.4:c.5331T>C	XP_006717948.1:p.Asn1777=
XM_006717888.4:c.5328T>C	XP_006717951.1:p.Asn1776=
XM_006717889.4:c.5283T>C	XP_006717952.1:p.Asn1761=
XM_006717890.3:c.4407T>C	XP_006717953.1:p.Asn1469=
XM_011539849.3:c.5331T>C	XP_011538151.1:p.Asn1777=
XM_011539850.3:c.4176T>C	XP_011538152.1:p.Asn1392=
XM_017016310.2:c.5331T>C	XP_016871799.1:p.Asn1777=
XM_017016311.2:c.5331T>C	XP_016871800.1:p.Asn1777=
XM_017016312.2:c.4317T>C	XP_016871801.1:p.Asn1439=
NM_001288989.2:c.5241T>C	NP_001275918.1:p.Asn1747=
NM_016341.4:c.5289T>C MANE Select	NP_057425.3:p.Asn1763=