Canonical Allele Identifier: CA211618553

Gene: PLCE1 NOC3L

Linked Data

• dbSNP Id: rs982930679
• MyVariant Identifiers: chr10:g.96081641T>C (hg19) ; chr10:g.94321884T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94321884T>C , CM000672.2:g.94321884T>C	GRCh38
NC_000010.10:g.96081641T>C , CM000672.1:g.96081641T>C	GRCh37
NC_000010.9:g.96071631T>C	NCBI36
NG_015799.1:g.332896T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371375.2:c.5419-17T>C (PLCE1)	ENSP00000360426.1:n.5419-17T>C
ENST00000685132.1:n.3742-17T>C (PLCE1)
ENST00000685253.1:c.*2886-17T>C (PLCE1)	ENSP00000509405.1:n.*2886-17T>C
ENST00000685889.1:n.3078-17T>C (PLCE1)
ENST00000686807.1:n.1762-17T>C (PLCE1)
ENST00000686954.1:c.*1627-17T>C (PLCE1)	ENSP00000508416.1:n.*1627-17T>C
ENST00000688810.1:c.5371-17T>C (PLCE1)	ENSP00000509140.1:n.5371-17T>C
ENST00000689233.1:n.10551-17T>C (PLCE1)
ENST00000690340.1:n.4016-17T>C (PLCE1)
ENST00000692286.1:c.6211-17T>C (PLCE1)	ENSP00000509490.1:n.6211-17T>C
ENST00000692396.1:c.6295-17T>C (PLCE1)	ENSP00000508605.1:n.6295-17T>C
ENST00000371380.8:c.6343-17T>C (PLCE1) MANE Select	ENSP00000360431.2:n.6343-17T>C
ENST00000371385.8:c.5317-17T>C (PLCE1)	ENSP00000360438.4:n.5317-17T>C
ENST00000674738.1:c.4898-17T>C (PLCE1)
ENST00000674827.1:c.4459-17T>C (PLCE1)	ENSP00000502523.1:n.4459-17T>C
ENST00000675218.1:c.5419-17T>C (PLCE1)	ENSP00000501910.1:n.5419-17T>C
ENST00000675487.1:c.*2276-17T>C (PLCE1)	ENSP00000502340.1:n.*2276-17T>C
ENST00000675718.1:c.5612-17T>C (PLCE1)
ENST00000260766.7:c.6343-17T>C (PLCE1)	ENSP00000260766.3:n.6343-17T>C
ENST00000371375.1:c.5419-17T>C (PLCE1)	ENSP00000360426.1:n.5419-17T>C
ENST00000371380.7:c.6343-17T>C (PLCE1)	ENSP00000360431.2:n.6343-17T>C
ENST00000371385.7:c.5419-17T>C (PLCE1)	ENSP00000360438.3:n.5419-17T>C
NM_001165979.2:c.5419-17T>C (PLCE1)	NP_001159451.1:n.5419-17T>C
NM_001288989.1:c.6295-17T>C (PLCE1)	NP_001275918.1:n.6295-17T>C
NM_016341.3:c.6343-17T>C (PLCE1)	NP_057425.3:n.6343-17T>C
XM_006717885.2:c.6385-17T>C (PLCE1)	XP_006717948.1:n.6385-17T>C
XM_006717886.2:c.6385-17T>C (PLCE1)	XP_006717949.1:n.6385-17T>C
XM_006717888.2:c.6382-17T>C (PLCE1)	XP_006717951.1:n.6382-17T>C
XM_006717889.2:c.6337-17T>C (PLCE1)	XP_006717952.1:n.6337-17T>C
XM_006717890.1:c.5461-17T>C (PLCE1)	XP_006717953.1:n.5461-17T>C
XM_011539849.1:c.6385-17T>C (PLCE1)	XP_011538151.1:n.6385-17T>C
XM_011539850.1:c.5230-17T>C (PLCE1)	XP_011538152.1:n.5230-17T>C
XR_945799.1:n.3311-6420A>G (NOC3L)
XM_006717885.4:c.6385-17T>C (PLCE1)	XP_006717948.1:n.6385-17T>C
XM_006717888.4:c.6382-17T>C (PLCE1)	XP_006717951.1:n.6382-17T>C
XM_006717889.4:c.6337-17T>C (PLCE1)	XP_006717952.1:n.6337-17T>C
XM_006717890.3:c.5461-17T>C (PLCE1)	XP_006717953.1:n.5461-17T>C
XM_011539849.3:c.6385-17T>C (PLCE1)	XP_011538151.1:n.6385-17T>C
XM_011539850.3:c.5230-17T>C (PLCE1)	XP_011538152.1:n.5230-17T>C
XM_017016310.2:c.6385-17T>C (PLCE1)	XP_016871799.1:n.6385-17T>C
XM_017016311.2:c.6385-17T>C (PLCE1)	XP_016871800.1:n.6385-17T>C
XM_017016312.2:c.5371-17T>C (PLCE1)	XP_016871801.1:n.5371-17T>C
XR_002957007.1:n.3312-6420A>G (NOC3L)
NM_001288989.2:c.6295-17T>C (PLCE1)	NP_001275918.1:n.6295-17T>C
NM_016341.4:c.6343-17T>C (PLCE1) MANE Select	NP_057425.3:n.6343-17T>C