Canonical Allele Identifier: CA377642300

Gene: PLCE1

Linked Data

• MyVariant Identifiers: chr10:g.96058405G>T (hg19) ; chr10:g.94298648G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94298648G>T , CM000672.2:g.94298648G>T	GRCh38
NC_000010.10:g.96058405G>T , CM000672.1:g.96058405G>T	GRCh37
NC_000010.9:g.96048395G>T	NCBI36
NG_015799.1:g.309660G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.4513G>T	ENSP00000360426.1:p.Ala1505Ser
ENST00000685253.1:c.*1980G>T	ENSP00000509405.1:n.*1980G>T
ENST00000685889.1:n.2172G>T
ENST00000686807.1:n.856G>T
ENST00000686954.1:c.*721G>T	ENSP00000508416.1:n.*721G>T
ENST00000688810.1:c.4465G>T	ENSP00000509140.1:p.Ala1489Ser
ENST00000689233.1:n.9645G>T
ENST00000690340.1:n.3110G>T
ENST00000692286.1:c.5305G>T	ENSP00000509490.1:p.Ala1769Ser
ENST00000692396.1:c.5389G>T	ENSP00000508605.1:p.Ala1797Ser
ENST00000371380.8:c.5437G>T MANE Select	ENSP00000360431.2:p.Ala1813Ser
ENST00000371385.8:c.4411G>T	ENSP00000360438.4:p.Ala1471Ser
ENST00000674738.1:c.3992G>T
ENST00000674827.1:c.3553G>T	ENSP00000502523.1:p.Ala1185Ser
ENST00000675218.1:c.4513G>T	ENSP00000501910.1:p.Ala1505Ser
ENST00000675487.1:c.*1370G>T	ENSP00000502340.1:n.*1370G>T
ENST00000675718.1:c.4706G>T
ENST00000260766.7:c.5437G>T	ENSP00000260766.3:p.Ala1813Ser
ENST00000371375.1:c.4513G>T	ENSP00000360426.1:p.Ala1505Ser
ENST00000371380.7:c.5437G>T	ENSP00000360431.2:p.Ala1813Ser
ENST00000371385.7:c.4513G>T	ENSP00000360438.3:p.Ala1505Ser
NM_001165979.2:c.4513G>T	NP_001159451.1:p.Ala1505Ser
NM_001288989.1:c.5389G>T	NP_001275918.1:p.Ala1797Ser
NM_016341.3:c.5437G>T	NP_057425.3:p.Ala1813Ser
XM_006717885.2:c.5479G>T	XP_006717948.1:p.Ala1827Ser
XM_006717886.2:c.5479G>T	XP_006717949.1:p.Ala1827Ser
XM_006717888.2:c.5476G>T	XP_006717951.1:p.Ala1826Ser
XM_006717889.2:c.5431G>T	XP_006717952.1:p.Ala1811Ser
XM_006717890.1:c.4555G>T	XP_006717953.1:p.Ala1519Ser
XM_011539849.1:c.5479G>T	XP_011538151.1:p.Ala1827Ser
XM_011539850.1:c.4324G>T	XP_011538152.1:p.Ala1442Ser
XM_006717885.4:c.5479G>T	XP_006717948.1:p.Ala1827Ser
XM_006717888.4:c.5476G>T	XP_006717951.1:p.Ala1826Ser
XM_006717889.4:c.5431G>T	XP_006717952.1:p.Ala1811Ser
XM_006717890.3:c.4555G>T	XP_006717953.1:p.Ala1519Ser
XM_011539849.3:c.5479G>T	XP_011538151.1:p.Ala1827Ser
XM_011539850.3:c.4324G>T	XP_011538152.1:p.Ala1442Ser
XM_017016310.2:c.5479G>T	XP_016871799.1:p.Ala1827Ser
XM_017016311.2:c.5479G>T	XP_016871800.1:p.Ala1827Ser
XM_017016312.2:c.4465G>T	XP_016871801.1:p.Ala1489Ser
NM_001288989.2:c.5389G>T	NP_001275918.1:p.Ala1797Ser
NM_016341.4:c.5437G>T MANE Select	NP_057425.3:p.Ala1813Ser