Canonical Allele Identifier: CA1826051206

Gene: PLEC

Linked Data

• dbSNP Id: rs1827884085

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143933116_143933117insA , CM000670.2:g.143933116_143933117insA	GRCh38
NC_000008.10:g.145007284_145007285insA , CM000670.1:g.145007284_145007285insA	GRCh37
NC_000008.9:g.145079272_145079273insA	NCBI36
NG_012492.1:g.48629_48630insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528025.6:c.1551-6_1551-5insT	ENSP00000437303.2:n.1551-6_1551-5insT
ENST00000685198.1:c.1470-6_1470-5insT	ENSP00000510528.1:n.1470-6_1470-5insT
ENST00000687971.1:c.1137-6_1137-5insT	ENSP00000510788.1:n.1137-6_1137-5insT
ENST00000693060.1:c.1350-6_1350-5insT	ENSP00000510329.1:n.1350-6_1350-5insT
ENST00000345136.8:c.1419-6_1419-5insT MANE Select	ENSP00000344848.3:n.1419-6_1419-5insT
ENST00000527303.2:c.1500-6_1500-5insT	ENSP00000433982.2:n.1500-6_1500-5insT
ENST00000322810.8:c.1830-6_1830-5insT	ENSP00000323856.4:n.1830-6_1830-5insT
ENST00000345136.7:c.1419-6_1419-5insT	ENSP00000344848.3:n.1419-6_1419-5insT
ENST00000354589.7:c.1419-6_1419-5insT	ENSP00000346602.3:n.1419-6_1419-5insT
ENST00000354958.6:c.1353-6_1353-5insT	ENSP00000347044.2:n.1353-6_1353-5insT
ENST00000356346.7:c.1377-6_1377-5insT MANE Plus Clinical	ENSP00000348702.3:n.1377-6_1377-5insT
ENST00000357649.6:c.1431-6_1431-5insT	ENSP00000350277.2:n.1431-6_1431-5insT
ENST00000398774.6:c.1323-6_1323-5insT	ENSP00000381756.2:n.1323-6_1323-5insT
ENST00000436759.6:c.1500-6_1500-5insT	ENSP00000388180.2:n.1500-6_1500-5insT
ENST00000527096.5:c.1488-6_1488-5insT	ENSP00000434583.1:n.1488-6_1488-5insT
ENST00000528025.5:c.1551-6_1551-5insT	ENSP00000437303.1:n.1551-6_1551-5insT
NM_000445.4:c.1500-6_1500-5insT	NP_000436.2:n.1500-6_1500-5insT
NM_201378.3:c.1377-6_1377-5insT	NP_958780.1:n.1377-6_1377-5insT
NM_201379.2:c.1353-6_1353-5insT	NP_958781.1:n.1353-6_1353-5insT
NM_201380.3:c.1830-6_1830-5insT	NP_958782.1:n.1830-6_1830-5insT
NM_201381.2:c.1323-6_1323-5insT	NP_958783.1:n.1323-6_1323-5insT
NM_201382.3:c.1419-6_1419-5insT	NP_958784.1:n.1419-6_1419-5insT
NM_201383.2:c.1431-6_1431-5insT	NP_958785.1:n.1431-6_1431-5insT
NM_201384.2:c.1419-6_1419-5insT	NP_958786.1:n.1419-6_1419-5insT
XM_005250976.2:c.1845-6_1845-5insT	XP_005251033.1:n.1845-6_1845-5insT
XM_005250978.2:c.1446-6_1446-5insT	XP_005251035.1:n.1446-6_1446-5insT
XM_005250979.3:c.1434-6_1434-5insT	XP_005251036.1:n.1434-6_1434-5insT
XM_005250980.3:c.1434-6_1434-5insT	XP_005251037.1:n.1434-6_1434-5insT
XM_005250981.2:c.1392-6_1392-5insT	XP_005251038.1:n.1392-6_1392-5insT
XM_005250982.2:c.1368-6_1368-5insT	XP_005251039.1:n.1368-6_1368-5insT
XM_005250983.2:c.1350-6_1350-5insT	XP_005251040.1:n.1350-6_1350-5insT
XM_005250984.3:c.1338-6_1338-5insT	XP_005251041.1:n.1338-6_1338-5insT
XM_006716588.2:c.1515-6_1515-5insT	XP_006716651.1:n.1515-6_1515-5insT
XM_006716589.2:c.1365-6_1365-5insT	XP_006716652.1:n.1365-6_1365-5insT
XM_006716590.2:c.1365-6_1365-5insT	XP_006716653.1:n.1365-6_1365-5insT
XM_011517130.1:c.1434-6_1434-5insT	XP_011515432.1:n.1434-6_1434-5insT
XM_011517131.1:c.1350-6_1350-5insT	XP_011515433.1:n.1350-6_1350-5insT
XM_011517132.1:c.1446-6_1446-5insT	XP_011515434.1:n.1446-6_1446-5insT
XM_005250976.4:c.1845-6_1845-5insT	XP_005251033.1:n.1845-6_1845-5insT
XM_005250978.3:c.1446-6_1446-5insT	XP_005251035.1:n.1446-6_1446-5insT
XM_005250979.4:c.1434-6_1434-5insT	XP_005251036.1:n.1434-6_1434-5insT
XM_005250980.4:c.1434-6_1434-5insT	XP_005251037.1:n.1434-6_1434-5insT
XM_005250981.3:c.1392-6_1392-5insT	XP_005251038.1:n.1392-6_1392-5insT
XM_005250982.4:c.1368-6_1368-5insT	XP_005251039.1:n.1368-6_1368-5insT
XM_005250984.5:c.1338-6_1338-5insT	XP_005251041.1:n.1338-6_1338-5insT
XM_006716588.3:c.1515-6_1515-5insT	XP_006716651.1:n.1515-6_1515-5insT
XM_006716590.3:c.1365-6_1365-5insT	XP_006716653.1:n.1365-6_1365-5insT
XM_011517130.2:c.1434-6_1434-5insT	XP_011515432.1:n.1434-6_1434-5insT
XM_011517131.2:c.1350-6_1350-5insT	XP_011515433.1:n.1350-6_1350-5insT
XM_011517132.2:c.1446-6_1446-5insT	XP_011515434.1:n.1446-6_1446-5insT
NM_000445.5:c.1500-6_1500-5insT	NP_000436.2:n.1500-6_1500-5insT
NM_201378.4:c.1377-6_1377-5insT MANE Plus Clinical	NP_958780.1:n.1377-6_1377-5insT
NM_201379.3:c.1353-6_1353-5insT	NP_958781.1:n.1353-6_1353-5insT
NM_201380.4:c.1830-6_1830-5insT	NP_958782.1:n.1830-6_1830-5insT
NM_201381.3:c.1323-6_1323-5insT	NP_958783.1:n.1323-6_1323-5insT
NM_201382.4:c.1419-6_1419-5insT	NP_958784.1:n.1419-6_1419-5insT
NM_201383.3:c.1431-6_1431-5insT	NP_958785.1:n.1431-6_1431-5insT
NM_201384.3:c.1419-6_1419-5insT MANE Select	NP_958786.1:n.1419-6_1419-5insT