Canonical Allele Identifier: CA372474653

Gene: PLEC

Linked Data

• MyVariant Identifiers: chr8:g.144990598A>T (hg19) ; chr8:g.143916430A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143916430A>T , CM000670.2:g.143916430A>T	GRCh38
NC_000008.10:g.144990598A>T , CM000670.1:g.144990598A>T	GRCh37
NC_000008.9:g.145062586A>T	NCBI36
NG_012492.1:g.65316T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528025.6:c.13523T>A	ENSP00000437303.2:p.Leu4508Gln
ENST00000685198.1:c.13442T>A	ENSP00000510528.1:p.Leu4481Gln
ENST00000687971.1:c.13109T>A	ENSP00000510788.1:p.Leu4370Gln
ENST00000693060.1:c.13322T>A	ENSP00000510329.1:p.Leu4441Gln
ENST00000345136.8:c.13391T>A MANE Select	ENSP00000344848.3:p.Leu4464Gln
ENST00000527303.2:c.10091T>A	ENSP00000433982.2:p.Leu3364Gln
ENST00000322810.8:c.13802T>A	ENSP00000323856.4:p.Leu4601Gln
ENST00000345136.7:c.13391T>A	ENSP00000344848.3:p.Leu4464Gln
ENST00000354589.7:c.13391T>A	ENSP00000346602.3:p.Leu4464Gln
ENST00000354958.6:c.13325T>A	ENSP00000347044.2:p.Leu4442Gln
ENST00000356346.7:c.13349T>A MANE Plus Clinical	ENSP00000348702.3:p.Leu4450Gln
ENST00000357649.6:c.13403T>A	ENSP00000350277.2:p.Leu4468Gln
ENST00000398774.6:c.13295T>A	ENSP00000381756.2:p.Leu4432Gln
ENST00000436759.6:c.13472T>A	ENSP00000388180.2:p.Leu4491Gln
ENST00000527096.5:c.13460T>A	ENSP00000434583.1:p.Leu4487Gln
NM_000445.4:c.13472T>A	NP_000436.2:p.Leu4491Gln
NM_201378.3:c.13349T>A	NP_958780.1:p.Leu4450Gln
NM_201379.2:c.13325T>A	NP_958781.1:p.Leu4442Gln
NM_201380.3:c.13802T>A	NP_958782.1:p.Leu4601Gln
NM_201381.2:c.13295T>A	NP_958783.1:p.Leu4432Gln
NM_201382.3:c.13391T>A	NP_958784.1:p.Leu4464Gln
NM_201383.2:c.13403T>A	NP_958785.1:p.Leu4468Gln
NM_201384.2:c.13391T>A	NP_958786.1:p.Leu4464Gln
XM_005250976.2:c.13817T>A	XP_005251033.1:p.Leu4606Gln
XM_005250978.2:c.13418T>A	XP_005251035.1:p.Leu4473Gln
XM_005250979.3:c.13406T>A	XP_005251036.1:p.Leu4469Gln
XM_005250980.3:c.13406T>A	XP_005251037.1:p.Leu4469Gln
XM_005250981.2:c.13364T>A	XP_005251038.1:p.Leu4455Gln
XM_005250982.2:c.13340T>A	XP_005251039.1:p.Leu4447Gln
XM_005250983.2:c.13322T>A	XP_005251040.1:p.Leu4441Gln
XM_005250984.3:c.13310T>A	XP_005251041.1:p.Leu4437Gln
XM_006716588.2:c.13487T>A	XP_006716651.1:p.Leu4496Gln
XM_006716589.2:c.13337T>A	XP_006716652.1:p.Leu4446Gln
XM_006716590.2:c.13337T>A	XP_006716653.1:p.Leu4446Gln
XM_011517130.1:c.13406T>A	XP_011515432.1:p.Leu4469Gln
XM_011517131.1:c.13322T>A	XP_011515433.1:p.Leu4441Gln
XM_011517132.1:c.10037T>A	XP_011515434.1:p.Leu3346Gln
XM_005250976.4:c.13817T>A	XP_005251033.1:p.Leu4606Gln
XM_005250978.3:c.13418T>A	XP_005251035.1:p.Leu4473Gln
XM_005250979.4:c.13406T>A	XP_005251036.1:p.Leu4469Gln
XM_005250980.4:c.13406T>A	XP_005251037.1:p.Leu4469Gln
XM_005250981.3:c.13364T>A	XP_005251038.1:p.Leu4455Gln
XM_005250982.4:c.13340T>A	XP_005251039.1:p.Leu4447Gln
XM_005250984.5:c.13310T>A	XP_005251041.1:p.Leu4437Gln
XM_006716588.3:c.13487T>A	XP_006716651.1:p.Leu4496Gln
XM_006716590.3:c.13337T>A	XP_006716653.1:p.Leu4446Gln
XM_011517130.2:c.13406T>A	XP_011515432.1:p.Leu4469Gln
XM_011517131.2:c.13322T>A	XP_011515433.1:p.Leu4441Gln
XM_011517132.2:c.10037T>A	XP_011515434.1:p.Leu3346Gln
NM_000445.5:c.13472T>A	NP_000436.2:p.Leu4491Gln
NM_201378.4:c.13349T>A MANE Plus Clinical	NP_958780.1:p.Leu4450Gln
NM_201379.3:c.13325T>A	NP_958781.1:p.Leu4442Gln
NM_201380.4:c.13802T>A	NP_958782.1:p.Leu4601Gln
NM_201381.3:c.13295T>A	NP_958783.1:p.Leu4432Gln
NM_201382.4:c.13391T>A	NP_958784.1:p.Leu4464Gln
NM_201383.3:c.13403T>A	NP_958785.1:p.Leu4468Gln
NM_201384.3:c.13391T>A MANE Select	NP_958786.1:p.Leu4464Gln