Canonical Allele Identifier: CA372475917

Gene: PLEC

Linked Data

• MyVariant Identifiers: chr8:g.144990763T>C (hg19) ; chr8:g.143916595T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143916595T>C , CM000670.2:g.143916595T>C	GRCh38
NC_000008.10:g.144990763T>C , CM000670.1:g.144990763T>C	GRCh37
NC_000008.9:g.145062751T>C	NCBI36
NG_012492.1:g.65151A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528025.6:c.13358A>G	ENSP00000437303.2:p.Asp4453Gly
ENST00000685198.1:c.13277A>G	ENSP00000510528.1:p.Asp4426Gly
ENST00000687971.1:c.12944A>G	ENSP00000510788.1:p.Asp4315Gly
ENST00000693060.1:c.13157A>G	ENSP00000510329.1:p.Asp4386Gly
ENST00000345136.8:c.13226A>G MANE Select	ENSP00000344848.3:p.Asp4409Gly
ENST00000527303.2:c.9926A>G	ENSP00000433982.2:p.Asp3309Gly
ENST00000322810.8:c.13637A>G	ENSP00000323856.4:p.Asp4546Gly
ENST00000345136.7:c.13226A>G	ENSP00000344848.3:p.Asp4409Gly
ENST00000354589.7:c.13226A>G	ENSP00000346602.3:p.Asp4409Gly
ENST00000354958.6:c.13160A>G	ENSP00000347044.2:p.Asp4387Gly
ENST00000356346.7:c.13184A>G MANE Plus Clinical	ENSP00000348702.3:p.Asp4395Gly
ENST00000357649.6:c.13238A>G	ENSP00000350277.2:p.Asp4413Gly
ENST00000398774.6:c.13130A>G	ENSP00000381756.2:p.Asp4377Gly
ENST00000436759.6:c.13307A>G	ENSP00000388180.2:p.Asp4436Gly
ENST00000527096.5:c.13295A>G	ENSP00000434583.1:p.Asp4432Gly
NM_000445.4:c.13307A>G	NP_000436.2:p.Asp4436Gly
NM_201378.3:c.13184A>G	NP_958780.1:p.Asp4395Gly
NM_201379.2:c.13160A>G	NP_958781.1:p.Asp4387Gly
NM_201380.3:c.13637A>G	NP_958782.1:p.Asp4546Gly
NM_201381.2:c.13130A>G	NP_958783.1:p.Asp4377Gly
NM_201382.3:c.13226A>G	NP_958784.1:p.Asp4409Gly
NM_201383.2:c.13238A>G	NP_958785.1:p.Asp4413Gly
NM_201384.2:c.13226A>G	NP_958786.1:p.Asp4409Gly
XM_005250976.2:c.13652A>G	XP_005251033.1:p.Asp4551Gly
XM_005250978.2:c.13253A>G	XP_005251035.1:p.Asp4418Gly
XM_005250979.3:c.13241A>G	XP_005251036.1:p.Asp4414Gly
XM_005250980.3:c.13241A>G	XP_005251037.1:p.Asp4414Gly
XM_005250981.2:c.13199A>G	XP_005251038.1:p.Asp4400Gly
XM_005250982.2:c.13175A>G	XP_005251039.1:p.Asp4392Gly
XM_005250983.2:c.13157A>G	XP_005251040.1:p.Asp4386Gly
XM_005250984.3:c.13145A>G	XP_005251041.1:p.Asp4382Gly
XM_006716588.2:c.13322A>G	XP_006716651.1:p.Asp4441Gly
XM_006716589.2:c.13172A>G	XP_006716652.1:p.Asp4391Gly
XM_006716590.2:c.13172A>G	XP_006716653.1:p.Asp4391Gly
XM_011517130.1:c.13241A>G	XP_011515432.1:p.Asp4414Gly
XM_011517131.1:c.13157A>G	XP_011515433.1:p.Asp4386Gly
XM_011517132.1:c.9872A>G	XP_011515434.1:p.Asp3291Gly
XM_005250976.4:c.13652A>G	XP_005251033.1:p.Asp4551Gly
XM_005250978.3:c.13253A>G	XP_005251035.1:p.Asp4418Gly
XM_005250979.4:c.13241A>G	XP_005251036.1:p.Asp4414Gly
XM_005250980.4:c.13241A>G	XP_005251037.1:p.Asp4414Gly
XM_005250981.3:c.13199A>G	XP_005251038.1:p.Asp4400Gly
XM_005250982.4:c.13175A>G	XP_005251039.1:p.Asp4392Gly
XM_005250984.5:c.13145A>G	XP_005251041.1:p.Asp4382Gly
XM_006716588.3:c.13322A>G	XP_006716651.1:p.Asp4441Gly
XM_006716590.3:c.13172A>G	XP_006716653.1:p.Asp4391Gly
XM_011517130.2:c.13241A>G	XP_011515432.1:p.Asp4414Gly
XM_011517131.2:c.13157A>G	XP_011515433.1:p.Asp4386Gly
XM_011517132.2:c.9872A>G	XP_011515434.1:p.Asp3291Gly
NM_000445.5:c.13307A>G	NP_000436.2:p.Asp4436Gly
NM_201378.4:c.13184A>G MANE Plus Clinical	NP_958780.1:p.Asp4395Gly
NM_201379.3:c.13160A>G	NP_958781.1:p.Asp4387Gly
NM_201380.4:c.13637A>G	NP_958782.1:p.Asp4546Gly
NM_201381.3:c.13130A>G	NP_958783.1:p.Asp4377Gly
NM_201382.4:c.13226A>G	NP_958784.1:p.Asp4409Gly
NM_201383.3:c.13238A>G	NP_958785.1:p.Asp4413Gly
NM_201384.3:c.13226A>G MANE Select	NP_958786.1:p.Asp4409Gly