Canonical Allele Identifier: CA372563906

Gene: PLEC

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143927048G>A , CM000670.2:g.143927048G>A	GRCh38
NC_000008.10:g.145001216G>A , CM000670.1:g.145001216G>A	GRCh37
NC_000008.9:g.145073204G>A	NCBI36
NG_012492.1:g.54698C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_201384.3:c.3874C>T MANE Select	NP_958786.1:p.Gln1292Ter
ENST00000345136.8:c.3874C>T MANE Select	ENSP00000344848.3:p.Gln1292Ter
NM_201378.4:c.3832C>T MANE Plus Clinical	NP_958780.1:p.Gln1278Ter
ENST00000356346.7:c.3832C>T MANE Plus Clinical	ENSP00000348702.3:p.Gln1278Ter
NM_000445.4:c.3955C>T	NP_000436.2:p.Gln1319Ter
NM_000445.5:c.3955C>T	NP_000436.2:p.Gln1319Ter
NM_201378.3:c.3832C>T	NP_958780.1:p.Gln1278Ter
NM_201379.2:c.3808C>T	NP_958781.1:p.Gln1270Ter
NM_201379.3:c.3808C>T	NP_958781.1:p.Gln1270Ter
NM_201380.3:c.4285C>T	NP_958782.1:p.Gln1429Ter
NM_201380.4:c.4285C>T	NP_958782.1:p.Gln1429Ter
NM_201381.2:c.3778C>T	NP_958783.1:p.Gln1260Ter
NM_201381.3:c.3778C>T	NP_958783.1:p.Gln1260Ter
NM_201382.3:c.3874C>T	NP_958784.1:p.Gln1292Ter
NM_201382.4:c.3874C>T	NP_958784.1:p.Gln1292Ter
NM_201383.2:c.3886C>T	NP_958785.1:p.Gln1296Ter
NM_201383.3:c.3886C>T	NP_958785.1:p.Gln1296Ter
NM_201384.2:c.3874C>T	NP_958786.1:p.Gln1292Ter
ENST00000322810.8:c.4285C>T	ENSP00000323856.4:p.Gln1429Ter
ENST00000345136.7:c.3874C>T	ENSP00000344848.3:p.Gln1292Ter
ENST00000354589.7:c.3874C>T	ENSP00000346602.3:p.Gln1292Ter
ENST00000354958.6:c.3808C>T	ENSP00000347044.2:p.Gln1270Ter
ENST00000357649.6:c.3886C>T	ENSP00000350277.2:p.Gln1296Ter
ENST00000398774.6:c.3778C>T	ENSP00000381756.2:p.Gln1260Ter
ENST00000436759.6:c.3955C>T	ENSP00000388180.2:p.Gln1319Ter
ENST00000527096.5:c.3943C>T	ENSP00000434583.1:p.Gln1315Ter
ENST00000527303.2:c.3955C>T	ENSP00000433982.2:p.Gln1319Ter
ENST00000528025.6:c.4006C>T	ENSP00000437303.2:p.Gln1336Ter
ENST00000685198.1:c.3925C>T	ENSP00000510528.1:p.Gln1309Ter
ENST00000687971.1:c.3592C>T	ENSP00000510788.1:p.Gln1198Ter
ENST00000693060.1:c.3805C>T	ENSP00000510329.1:p.Gln1269Ter
XM_005250976.2:c.4300C>T	XP_005251033.1:p.Gln1434Ter
XM_005250976.4:c.4300C>T	XP_005251033.1:p.Gln1434Ter
XM_005250978.2:c.3901C>T	XP_005251035.1:p.Gln1301Ter
XM_005250978.3:c.3901C>T	XP_005251035.1:p.Gln1301Ter
XM_005250979.3:c.3889C>T	XP_005251036.1:p.Gln1297Ter
XM_005250979.4:c.3889C>T	XP_005251036.1:p.Gln1297Ter
XM_005250980.3:c.3889C>T	XP_005251037.1:p.Gln1297Ter
XM_005250980.4:c.3889C>T	XP_005251037.1:p.Gln1297Ter
XM_005250981.2:c.3847C>T	XP_005251038.1:p.Gln1283Ter
XM_005250981.3:c.3847C>T	XP_005251038.1:p.Gln1283Ter
XM_005250982.2:c.3823C>T	XP_005251039.1:p.Gln1275Ter
XM_005250982.4:c.3823C>T	XP_005251039.1:p.Gln1275Ter
XM_005250983.2:c.3805C>T	XP_005251040.1:p.Gln1269Ter
XM_005250984.3:c.3793C>T	XP_005251041.1:p.Gln1265Ter
XM_005250984.5:c.3793C>T	XP_005251041.1:p.Gln1265Ter
XM_006716588.2:c.3970C>T	XP_006716651.1:p.Gln1324Ter
XM_006716588.3:c.3970C>T	XP_006716651.1:p.Gln1324Ter
XM_006716589.2:c.3820C>T	XP_006716652.1:p.Gln1274Ter
XM_006716590.2:c.3820C>T	XP_006716653.1:p.Gln1274Ter
XM_006716590.3:c.3820C>T	XP_006716653.1:p.Gln1274Ter
XM_011517130.1:c.3889C>T	XP_011515432.1:p.Gln1297Ter
XM_011517130.2:c.3889C>T	XP_011515432.1:p.Gln1297Ter
XM_011517131.1:c.3805C>T	XP_011515433.1:p.Gln1269Ter
XM_011517131.2:c.3805C>T	XP_011515433.1:p.Gln1269Ter
XM_011517132.1:c.3901C>T	XP_011515434.1:p.Gln1301Ter
XM_011517132.2:c.3901C>T	XP_011515434.1:p.Gln1301Ter