Canonical Allele Identifier: CA4925099

Gene: PLEC

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143920778T>C , CM000670.2:g.143920778T>C	GRCh38
NC_000008.10:g.144994946T>C , CM000670.1:g.144994946T>C	GRCh37
NC_000008.9:g.145066934T>C	NCBI36
NG_012492.1:g.60968A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_201384.3:c.9043A>G MANE Select	NP_958786.1:p.Thr3015Ala
ENST00000345136.8:c.9043A>G MANE Select	ENSP00000344848.3:p.Thr3015Ala
NM_201378.4:c.9001A>G MANE Plus Clinical	NP_958780.1:p.Thr3001Ala
ENST00000356346.7:c.9001A>G MANE Plus Clinical	ENSP00000348702.3:p.Thr3001Ala
NM_000445.4:c.9124A>G	NP_000436.2:p.Thr3042Ala
NM_000445.5:c.9124A>G	NP_000436.2:p.Thr3042Ala
NM_201378.3:c.9001A>G	NP_958780.1:p.Thr3001Ala
NM_201379.2:c.8977A>G	NP_958781.1:p.Thr2993Ala
NM_201379.3:c.8977A>G	NP_958781.1:p.Thr2993Ala
NM_201380.3:c.9454A>G	NP_958782.1:p.Thr3152Ala
NM_201380.4:c.9454A>G	NP_958782.1:p.Thr3152Ala
NM_201381.2:c.8947A>G	NP_958783.1:p.Thr2983Ala
NM_201381.3:c.8947A>G	NP_958783.1:p.Thr2983Ala
NM_201382.3:c.9043A>G	NP_958784.1:p.Thr3015Ala
NM_201382.4:c.9043A>G	NP_958784.1:p.Thr3015Ala
NM_201383.2:c.9055A>G	NP_958785.1:p.Thr3019Ala
NM_201383.3:c.9055A>G	NP_958785.1:p.Thr3019Ala
NM_201384.2:c.9043A>G	NP_958786.1:p.Thr3015Ala
ENST00000322810.8:c.9454A>G	ENSP00000323856.4:p.Thr3152Ala
ENST00000345136.7:c.9043A>G	ENSP00000344848.3:p.Thr3015Ala
ENST00000354589.7:c.9043A>G	ENSP00000346602.3:p.Thr3015Ala
ENST00000354958.6:c.8977A>G	ENSP00000347044.2:p.Thr2993Ala
ENST00000357649.6:c.9055A>G	ENSP00000350277.2:p.Thr3019Ala
ENST00000398774.6:c.8947A>G	ENSP00000381756.2:p.Thr2983Ala
ENST00000436759.6:c.9124A>G	ENSP00000388180.2:p.Thr3042Ala
ENST00000527096.5:c.9112A>G	ENSP00000434583.1:p.Thr3038Ala
ENST00000527303.2:c.5743A>G	ENSP00000433982.2:p.Thr1915Ala
ENST00000528025.6:c.9175A>G	ENSP00000437303.2:p.Thr3059Ala
ENST00000685198.1:c.9094A>G	ENSP00000510528.1:p.Thr3032Ala
ENST00000687971.1:c.8761A>G	ENSP00000510788.1:p.Thr2921Ala
ENST00000693060.1:c.8974A>G	ENSP00000510329.1:p.Thr2992Ala
XM_005250976.2:c.9469A>G	XP_005251033.1:p.Thr3157Ala
XM_005250976.4:c.9469A>G	XP_005251033.1:p.Thr3157Ala
XM_005250978.2:c.9070A>G	XP_005251035.1:p.Thr3024Ala
XM_005250978.3:c.9070A>G	XP_005251035.1:p.Thr3024Ala
XM_005250979.3:c.9058A>G	XP_005251036.1:p.Thr3020Ala
XM_005250979.4:c.9058A>G	XP_005251036.1:p.Thr3020Ala
XM_005250980.3:c.9058A>G	XP_005251037.1:p.Thr3020Ala
XM_005250980.4:c.9058A>G	XP_005251037.1:p.Thr3020Ala
XM_005250981.2:c.9016A>G	XP_005251038.1:p.Thr3006Ala
XM_005250981.3:c.9016A>G	XP_005251038.1:p.Thr3006Ala
XM_005250982.2:c.8992A>G	XP_005251039.1:p.Thr2998Ala
XM_005250982.4:c.8992A>G	XP_005251039.1:p.Thr2998Ala
XM_005250983.2:c.8974A>G	XP_005251040.1:p.Thr2992Ala
XM_005250984.3:c.8962A>G	XP_005251041.1:p.Thr2988Ala
XM_005250984.5:c.8962A>G	XP_005251041.1:p.Thr2988Ala
XM_006716588.2:c.9139A>G	XP_006716651.1:p.Thr3047Ala
XM_006716588.3:c.9139A>G	XP_006716651.1:p.Thr3047Ala
XM_006716589.2:c.8989A>G	XP_006716652.1:p.Thr2997Ala
XM_006716590.2:c.8989A>G	XP_006716653.1:p.Thr2997Ala
XM_006716590.3:c.8989A>G	XP_006716653.1:p.Thr2997Ala
XM_011517130.1:c.9058A>G	XP_011515432.1:p.Thr3020Ala
XM_011517130.2:c.9058A>G	XP_011515432.1:p.Thr3020Ala
XM_011517131.1:c.8974A>G	XP_011515433.1:p.Thr2992Ala
XM_011517131.2:c.8974A>G	XP_011515433.1:p.Thr2992Ala
XM_011517132.1:c.5689A>G	XP_011515434.1:p.Thr1897Ala
XM_011517132.2:c.5689A>G	XP_011515434.1:p.Thr1897Ala