Canonical Allele Identifier: CA1826037486

Gene: PLEC

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143916615C= , CM000670.2:g.143916615C=	GRCh38
NC_000008.10:g.144990783C= , CM000670.1:g.144990783C=	GRCh37
NC_000008.9:g.145062771C=	NCBI36
NG_012492.1:g.65131G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528025.6:c.13338G=	ENSP00000437303.2:p.Thr4446=
ENST00000685198.1:c.13257G=	ENSP00000510528.1:p.Thr4419=
ENST00000687971.1:c.12924G=	ENSP00000510788.1:p.Thr4308=
ENST00000693060.1:c.13137G=	ENSP00000510329.1:p.Thr4379=
ENST00000345136.8:c.13206G= MANE Select	ENSP00000344848.3:p.Thr4402=
ENST00000527303.2:c.9906G=	ENSP00000433982.2:p.Thr3302=
ENST00000322810.8:c.13617G=	ENSP00000323856.4:p.Thr4539=
ENST00000345136.7:c.13206G=	ENSP00000344848.3:p.Thr4402=
ENST00000354589.7:c.13206G=	ENSP00000346602.3:p.Thr4402=
ENST00000354958.6:c.13140G=	ENSP00000347044.2:p.Thr4380=
ENST00000356346.7:c.13164G= MANE Plus Clinical	ENSP00000348702.3:p.Thr4388=
ENST00000357649.6:c.13218G=	ENSP00000350277.2:p.Thr4406=
ENST00000398774.6:c.13110G=	ENSP00000381756.2:p.Thr4370=
ENST00000436759.6:c.13287G=	ENSP00000388180.2:p.Thr4429=
ENST00000527096.5:c.13275G=	ENSP00000434583.1:p.Thr4425=
NM_000445.4:c.13287G=	NP_000436.2:p.Thr4429=
NM_201378.3:c.13164G=	NP_958780.1:p.Thr4388=
NM_201379.2:c.13140G=	NP_958781.1:p.Thr4380=
NM_201380.3:c.13617G=	NP_958782.1:p.Thr4539=
NM_201381.2:c.13110G=	NP_958783.1:p.Thr4370=
NM_201382.3:c.13206G=	NP_958784.1:p.Thr4402=
NM_201383.2:c.13218G=	NP_958785.1:p.Thr4406=
NM_201384.2:c.13206G=	NP_958786.1:p.Thr4402=
XM_005250976.2:c.13632G=	XP_005251033.1:p.Thr4544=
XM_005250978.2:c.13233G=	XP_005251035.1:p.Thr4411=
XM_005250979.3:c.13221G=	XP_005251036.1:p.Thr4407=
XM_005250980.3:c.13221G=	XP_005251037.1:p.Thr4407=
XM_005250981.2:c.13179G=	XP_005251038.1:p.Thr4393=
XM_005250982.2:c.13155G=	XP_005251039.1:p.Thr4385=
XM_005250983.2:c.13137G=	XP_005251040.1:p.Thr4379=
XM_005250984.3:c.13125G=	XP_005251041.1:p.Thr4375=
XM_006716588.2:c.13302G=	XP_006716651.1:p.Thr4434=
XM_006716589.2:c.13152G=	XP_006716652.1:p.Thr4384=
XM_006716590.2:c.13152G=	XP_006716653.1:p.Thr4384=
XM_011517130.1:c.13221G=	XP_011515432.1:p.Thr4407=
XM_011517131.1:c.13137G=	XP_011515433.1:p.Thr4379=
XM_011517132.1:c.9852G=	XP_011515434.1:p.Thr3284=
XM_005250976.4:c.13632G=	XP_005251033.1:p.Thr4544=
XM_005250978.3:c.13233G=	XP_005251035.1:p.Thr4411=
XM_005250979.4:c.13221G=	XP_005251036.1:p.Thr4407=
XM_005250980.4:c.13221G=	XP_005251037.1:p.Thr4407=
XM_005250981.3:c.13179G=	XP_005251038.1:p.Thr4393=
XM_005250982.4:c.13155G=	XP_005251039.1:p.Thr4385=
XM_005250984.5:c.13125G=	XP_005251041.1:p.Thr4375=
XM_006716588.3:c.13302G=	XP_006716651.1:p.Thr4434=
XM_006716590.3:c.13152G=	XP_006716653.1:p.Thr4384=
XM_011517130.2:c.13221G=	XP_011515432.1:p.Thr4407=
XM_011517131.2:c.13137G=	XP_011515433.1:p.Thr4379=
XM_011517132.2:c.9852G=	XP_011515434.1:p.Thr3284=
NM_000445.5:c.13287G=	NP_000436.2:p.Thr4429=
NM_201378.4:c.13164G= MANE Plus Clinical	NP_958780.1:p.Thr4388=
NM_201379.3:c.13140G=	NP_958781.1:p.Thr4380=
NM_201380.4:c.13617G=	NP_958782.1:p.Thr4539=
NM_201381.3:c.13110G=	NP_958783.1:p.Thr4370=
NM_201382.4:c.13206G=	NP_958784.1:p.Thr4402=
NM_201383.3:c.13218G=	NP_958785.1:p.Thr4406=
NM_201384.3:c.13206G= MANE Select	NP_958786.1:p.Thr4402=