Canonical Allele Identifier: CA1826049368

Gene: PLEC

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143930163C= , CM000670.2:g.143930163C=	GRCh38
NC_000008.10:g.145004331C= , CM000670.1:g.145004331C=	GRCh37
NC_000008.9:g.145076319C=	NCBI36
NG_012492.1:g.51583G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528025.6:c.2725G=	ENSP00000437303.2:p.Ala909=
ENST00000685198.1:c.2644G=	ENSP00000510528.1:p.Ala882=
ENST00000687971.1:c.2311G=	ENSP00000510788.1:p.Ala771=
ENST00000693060.1:c.2524G=	ENSP00000510329.1:p.Ala842=
ENST00000345136.8:c.2593G= MANE Select	ENSP00000344848.3:p.Ala865=
ENST00000527303.2:c.2674G=	ENSP00000433982.2:p.Ala892=
ENST00000322810.8:c.3004G=	ENSP00000323856.4:p.Ala1002=
ENST00000345136.7:c.2593G=	ENSP00000344848.3:p.Ala865=
ENST00000354589.7:c.2593G=	ENSP00000346602.3:p.Ala865=
ENST00000354958.6:c.2527G=	ENSP00000347044.2:p.Ala843=
ENST00000356346.7:c.2551G= MANE Plus Clinical	ENSP00000348702.3:p.Ala851=
ENST00000357649.6:c.2605G=	ENSP00000350277.2:p.Ala869=
ENST00000398774.6:c.2497G=	ENSP00000381756.2:p.Ala833=
ENST00000436759.6:c.2674G=	ENSP00000388180.2:p.Ala892=
ENST00000527096.5:c.2662G=	ENSP00000434583.1:p.Ala888=
NM_000445.4:c.2674G=	NP_000436.2:p.Ala892=
NM_201378.3:c.2551G=	NP_958780.1:p.Ala851=
NM_201379.2:c.2527G=	NP_958781.1:p.Ala843=
NM_201380.3:c.3004G=	NP_958782.1:p.Ala1002=
NM_201381.2:c.2497G=	NP_958783.1:p.Ala833=
NM_201382.3:c.2593G=	NP_958784.1:p.Ala865=
NM_201383.2:c.2605G=	NP_958785.1:p.Ala869=
NM_201384.2:c.2593G=	NP_958786.1:p.Ala865=
XM_005250976.2:c.3019G=	XP_005251033.1:p.Ala1007=
XM_005250978.2:c.2620G=	XP_005251035.1:p.Ala874=
XM_005250979.3:c.2608G=	XP_005251036.1:p.Ala870=
XM_005250980.3:c.2608G=	XP_005251037.1:p.Ala870=
XM_005250981.2:c.2566G=	XP_005251038.1:p.Ala856=
XM_005250982.2:c.2542G=	XP_005251039.1:p.Ala848=
XM_005250983.2:c.2524G=	XP_005251040.1:p.Ala842=
XM_005250984.3:c.2512G=	XP_005251041.1:p.Ala838=
XM_006716588.2:c.2689G=	XP_006716651.1:p.Ala897=
XM_006716589.2:c.2539G=	XP_006716652.1:p.Ala847=
XM_006716590.2:c.2539G=	XP_006716653.1:p.Ala847=
XM_011517130.1:c.2608G=	XP_011515432.1:p.Ala870=
XM_011517131.1:c.2524G=	XP_011515433.1:p.Ala842=
XM_011517132.1:c.2620G=	XP_011515434.1:p.Ala874=
XM_005250976.4:c.3019G=	XP_005251033.1:p.Ala1007=
XM_005250978.3:c.2620G=	XP_005251035.1:p.Ala874=
XM_005250979.4:c.2608G=	XP_005251036.1:p.Ala870=
XM_005250980.4:c.2608G=	XP_005251037.1:p.Ala870=
XM_005250981.3:c.2566G=	XP_005251038.1:p.Ala856=
XM_005250982.4:c.2542G=	XP_005251039.1:p.Ala848=
XM_005250984.5:c.2512G=	XP_005251041.1:p.Ala838=
XM_006716588.3:c.2689G=	XP_006716651.1:p.Ala897=
XM_006716590.3:c.2539G=	XP_006716653.1:p.Ala847=
XM_011517130.2:c.2608G=	XP_011515432.1:p.Ala870=
XM_011517131.2:c.2524G=	XP_011515433.1:p.Ala842=
XM_011517132.2:c.2620G=	XP_011515434.1:p.Ala874=
NM_000445.5:c.2674G=	NP_000436.2:p.Ala892=
NM_201378.4:c.2551G= MANE Plus Clinical	NP_958780.1:p.Ala851=
NM_201379.3:c.2527G=	NP_958781.1:p.Ala843=
NM_201380.4:c.3004G=	NP_958782.1:p.Ala1002=
NM_201381.3:c.2497G=	NP_958783.1:p.Ala833=
NM_201382.4:c.2593G=	NP_958784.1:p.Ala865=
NM_201383.3:c.2605G=	NP_958785.1:p.Ala869=
NM_201384.3:c.2593G= MANE Select	NP_958786.1:p.Ala865=