Canonical Allele Identifier: CA377641911

Gene: PLCE1

Linked Data

• dbSNP Id: rs1228062735
• gnomAD v3: 10-94298499-A-T
• gnomAD v4: 10-94298499-A-T
• MyVariant Identifiers: chr10:g.96058256A>T (hg19) ; chr10:g.94298499A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298499A>T , CM000672.2:g.94298499A>T	GRCh38
NC_000010.10:g.96058256A>T , CM000672.1:g.96058256A>T	GRCh37
NC_000010.9:g.96048246A>T	NCBI36
NG_015799.1:g.309511A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4364A>T	ENSP00000360426.1:p.Asn1455Ile
ENST00000685253.1:c.*1831A>T	ENSP00000509405.1:n.*1831A>T
ENST00000685889.1:n.2023A>T
ENST00000686807.1:n.707A>T
ENST00000686954.1:c.*572A>T	ENSP00000508416.1:n.*572A>T
ENST00000688810.1:c.4316A>T	ENSP00000509140.1:p.Asn1439Ile
ENST00000689233.1:n.9496A>T
ENST00000690340.1:n.2961A>T
ENST00000692286.1:c.5156A>T	ENSP00000509490.1:p.Asn1719Ile
ENST00000692396.1:c.5240A>T	ENSP00000508605.1:p.Asn1747Ile
ENST00000371380.8:c.5288A>T MANE Select	ENSP00000360431.2:p.Asn1763Ile
ENST00000371385.8:c.4262A>T	ENSP00000360438.4:p.Asn1421Ile
ENST00000674738.1:c.3843A>T
ENST00000674827.1:c.3404A>T	ENSP00000502523.1:p.Asn1135Ile
ENST00000675218.1:c.4364A>T	ENSP00000501910.1:p.Asn1455Ile
ENST00000675487.1:c.*1221A>T	ENSP00000502340.1:n.*1221A>T
ENST00000675718.1:c.4557A>T
ENST00000260766.7:c.5288A>T	ENSP00000260766.3:p.Asn1763Ile
ENST00000371375.1:c.4364A>T	ENSP00000360426.1:p.Asn1455Ile
ENST00000371380.7:c.5288A>T	ENSP00000360431.2:p.Asn1763Ile
ENST00000371385.7:c.4364A>T	ENSP00000360438.3:p.Asn1455Ile
NM_001165979.2:c.4364A>T	NP_001159451.1:p.Asn1455Ile
NM_001288989.1:c.5240A>T	NP_001275918.1:p.Asn1747Ile
NM_016341.3:c.5288A>T	NP_057425.3:p.Asn1763Ile
XM_006717885.2:c.5330A>T	XP_006717948.1:p.Asn1777Ile
XM_006717886.2:c.5330A>T	XP_006717949.1:p.Asn1777Ile
XM_006717888.2:c.5327A>T	XP_006717951.1:p.Asn1776Ile
XM_006717889.2:c.5282A>T	XP_006717952.1:p.Asn1761Ile
XM_006717890.1:c.4406A>T	XP_006717953.1:p.Asn1469Ile
XM_011539849.1:c.5330A>T	XP_011538151.1:p.Asn1777Ile
XM_011539850.1:c.4175A>T	XP_011538152.1:p.Asn1392Ile
XM_006717885.4:c.5330A>T	XP_006717948.1:p.Asn1777Ile
XM_006717888.4:c.5327A>T	XP_006717951.1:p.Asn1776Ile
XM_006717889.4:c.5282A>T	XP_006717952.1:p.Asn1761Ile
XM_006717890.3:c.4406A>T	XP_006717953.1:p.Asn1469Ile
XM_011539849.3:c.5330A>T	XP_011538151.1:p.Asn1777Ile
XM_011539850.3:c.4175A>T	XP_011538152.1:p.Asn1392Ile
XM_017016310.2:c.5330A>T	XP_016871799.1:p.Asn1777Ile
XM_017016311.2:c.5330A>T	XP_016871800.1:p.Asn1777Ile
XM_017016312.2:c.4316A>T	XP_016871801.1:p.Asn1439Ile
NM_001288989.2:c.5240A>T	NP_001275918.1:p.Asn1747Ile
NM_016341.4:c.5288A>T MANE Select	NP_057425.3:p.Asn1763Ile