Canonical Allele Identifier: CA187619339

Gene: PLEC

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143930197G>A , CM000670.2:g.143930197G>A	GRCh38
NC_000008.10:g.145004365G>A , CM000670.1:g.145004365G>A	GRCh37
NC_000008.9:g.145076353G>A	NCBI36
NG_012492.1:g.51549C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_201384.3:c.2559C>T MANE Select	NP_958786.1:p.Ser853=
ENST00000345136.8:c.2559C>T MANE Select	ENSP00000344848.3:p.Ser853=
NM_201378.4:c.2517C>T MANE Plus Clinical	NP_958780.1:p.Ser839=
ENST00000356346.7:c.2517C>T MANE Plus Clinical	ENSP00000348702.3:p.Ser839=
NM_000445.4:c.2640C>T	NP_000436.2:p.Ser880=
NM_000445.5:c.2640C>T	NP_000436.2:p.Ser880=
NM_201378.3:c.2517C>T	NP_958780.1:p.Ser839=
NM_201379.2:c.2493C>T	NP_958781.1:p.Ser831=
NM_201379.3:c.2493C>T	NP_958781.1:p.Ser831=
NM_201380.3:c.2970C>T	NP_958782.1:p.Ser990=
NM_201380.4:c.2970C>T	NP_958782.1:p.Ser990=
NM_201381.2:c.2463C>T	NP_958783.1:p.Ser821=
NM_201381.3:c.2463C>T	NP_958783.1:p.Ser821=
NM_201382.3:c.2559C>T	NP_958784.1:p.Ser853=
NM_201382.4:c.2559C>T	NP_958784.1:p.Ser853=
NM_201383.2:c.2571C>T	NP_958785.1:p.Ser857=
NM_201383.3:c.2571C>T	NP_958785.1:p.Ser857=
NM_201384.2:c.2559C>T	NP_958786.1:p.Ser853=
ENST00000322810.8:c.2970C>T	ENSP00000323856.4:p.Ser990=
ENST00000345136.7:c.2559C>T	ENSP00000344848.3:p.Ser853=
ENST00000354589.7:c.2559C>T	ENSP00000346602.3:p.Ser853=
ENST00000354958.6:c.2493C>T	ENSP00000347044.2:p.Ser831=
ENST00000357649.6:c.2571C>T	ENSP00000350277.2:p.Ser857=
ENST00000398774.6:c.2463C>T	ENSP00000381756.2:p.Ser821=
ENST00000436759.6:c.2640C>T	ENSP00000388180.2:p.Ser880=
ENST00000527096.5:c.2628C>T	ENSP00000434583.1:p.Ser876=
ENST00000527303.2:c.2640C>T	ENSP00000433982.2:p.Ser880=
ENST00000528025.6:c.2691C>T	ENSP00000437303.2:p.Ser897=
ENST00000685198.1:c.2610C>T	ENSP00000510528.1:p.Ser870=
ENST00000687971.1:c.2277C>T	ENSP00000510788.1:p.Ser759=
ENST00000693060.1:c.2490C>T	ENSP00000510329.1:p.Ser830=
XM_005250976.2:c.2985C>T	XP_005251033.1:p.Ser995=
XM_005250976.4:c.2985C>T	XP_005251033.1:p.Ser995=
XM_005250978.2:c.2586C>T	XP_005251035.1:p.Ser862=
XM_005250978.3:c.2586C>T	XP_005251035.1:p.Ser862=
XM_005250979.3:c.2574C>T	XP_005251036.1:p.Ser858=
XM_005250979.4:c.2574C>T	XP_005251036.1:p.Ser858=
XM_005250980.3:c.2574C>T	XP_005251037.1:p.Ser858=
XM_005250980.4:c.2574C>T	XP_005251037.1:p.Ser858=
XM_005250981.2:c.2532C>T	XP_005251038.1:p.Ser844=
XM_005250981.3:c.2532C>T	XP_005251038.1:p.Ser844=
XM_005250982.2:c.2508C>T	XP_005251039.1:p.Ser836=
XM_005250982.4:c.2508C>T	XP_005251039.1:p.Ser836=
XM_005250983.2:c.2490C>T	XP_005251040.1:p.Ser830=
XM_005250984.3:c.2478C>T	XP_005251041.1:p.Ser826=
XM_005250984.5:c.2478C>T	XP_005251041.1:p.Ser826=
XM_006716588.2:c.2655C>T	XP_006716651.1:p.Ser885=
XM_006716588.3:c.2655C>T	XP_006716651.1:p.Ser885=
XM_006716589.2:c.2505C>T	XP_006716652.1:p.Ser835=
XM_006716590.2:c.2505C>T	XP_006716653.1:p.Ser835=
XM_006716590.3:c.2505C>T	XP_006716653.1:p.Ser835=
XM_011517130.1:c.2574C>T	XP_011515432.1:p.Ser858=
XM_011517130.2:c.2574C>T	XP_011515432.1:p.Ser858=
XM_011517131.1:c.2490C>T	XP_011515433.1:p.Ser830=
XM_011517131.2:c.2490C>T	XP_011515433.1:p.Ser830=
XM_011517132.1:c.2586C>T	XP_011515434.1:p.Ser862=
XM_011517132.2:c.2586C>T	XP_011515434.1:p.Ser862=