Canonical Allele Identifier: CA372474128

Gene: PLEC

Linked Data

• gnomAD v4: 8-143916319-G-A
• MyVariant Identifiers: chr8:g.144990487G>A (hg19) ; chr8:g.143916319G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143916319G>A , CM000670.2:g.143916319G>A	GRCh38
NC_000008.10:g.144990487G>A , CM000670.1:g.144990487G>A	GRCh37
NC_000008.9:g.145062475G>A	NCBI36
NG_012492.1:g.65427C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528025.6:c.13634C>T	ENSP00000437303.2:p.Ser4545Phe
ENST00000685198.1:c.13553C>T	ENSP00000510528.1:p.Ser4518Phe
ENST00000687971.1:c.13220C>T	ENSP00000510788.1:p.Ser4407Phe
ENST00000693060.1:c.13433C>T	ENSP00000510329.1:p.Ser4478Phe
ENST00000345136.8:c.13502C>T MANE Select	ENSP00000344848.3:p.Ser4501Phe
ENST00000527303.2:c.10202C>T	ENSP00000433982.2:p.Ser3401Phe
ENST00000322810.8:c.13913C>T	ENSP00000323856.4:p.Ser4638Phe
ENST00000345136.7:c.13502C>T	ENSP00000344848.3:p.Ser4501Phe
ENST00000354589.7:c.13502C>T	ENSP00000346602.3:p.Ser4501Phe
ENST00000354958.6:c.13436C>T	ENSP00000347044.2:p.Ser4479Phe
ENST00000356346.7:c.13460C>T MANE Plus Clinical	ENSP00000348702.3:p.Ser4487Phe
ENST00000357649.6:c.13514C>T	ENSP00000350277.2:p.Ser4505Phe
ENST00000398774.6:c.13406C>T	ENSP00000381756.2:p.Ser4469Phe
ENST00000436759.6:c.13583C>T	ENSP00000388180.2:p.Ser4528Phe
ENST00000527096.5:c.13571C>T	ENSP00000434583.1:p.Ser4524Phe
NM_000445.4:c.13583C>T	NP_000436.2:p.Ser4528Phe
NM_201378.3:c.13460C>T	NP_958780.1:p.Ser4487Phe
NM_201379.2:c.13436C>T	NP_958781.1:p.Ser4479Phe
NM_201380.3:c.13913C>T	NP_958782.1:p.Ser4638Phe
NM_201381.2:c.13406C>T	NP_958783.1:p.Ser4469Phe
NM_201382.3:c.13502C>T	NP_958784.1:p.Ser4501Phe
NM_201383.2:c.13514C>T	NP_958785.1:p.Ser4505Phe
NM_201384.2:c.13502C>T	NP_958786.1:p.Ser4501Phe
XM_005250976.2:c.13928C>T	XP_005251033.1:p.Ser4643Phe
XM_005250978.2:c.13529C>T	XP_005251035.1:p.Ser4510Phe
XM_005250979.3:c.13517C>T	XP_005251036.1:p.Ser4506Phe
XM_005250980.3:c.13517C>T	XP_005251037.1:p.Ser4506Phe
XM_005250981.2:c.13475C>T	XP_005251038.1:p.Ser4492Phe
XM_005250982.2:c.13451C>T	XP_005251039.1:p.Ser4484Phe
XM_005250983.2:c.13433C>T	XP_005251040.1:p.Ser4478Phe
XM_005250984.3:c.13421C>T	XP_005251041.1:p.Ser4474Phe
XM_006716588.2:c.13598C>T	XP_006716651.1:p.Ser4533Phe
XM_006716589.2:c.13448C>T	XP_006716652.1:p.Ser4483Phe
XM_006716590.2:c.13448C>T	XP_006716653.1:p.Ser4483Phe
XM_011517130.1:c.13517C>T	XP_011515432.1:p.Ser4506Phe
XM_011517131.1:c.13433C>T	XP_011515433.1:p.Ser4478Phe
XM_011517132.1:c.10148C>T	XP_011515434.1:p.Ser3383Phe
XM_005250976.4:c.13928C>T	XP_005251033.1:p.Ser4643Phe
XM_005250978.3:c.13529C>T	XP_005251035.1:p.Ser4510Phe
XM_005250979.4:c.13517C>T	XP_005251036.1:p.Ser4506Phe
XM_005250980.4:c.13517C>T	XP_005251037.1:p.Ser4506Phe
XM_005250981.3:c.13475C>T	XP_005251038.1:p.Ser4492Phe
XM_005250982.4:c.13451C>T	XP_005251039.1:p.Ser4484Phe
XM_005250984.5:c.13421C>T	XP_005251041.1:p.Ser4474Phe
XM_006716588.3:c.13598C>T	XP_006716651.1:p.Ser4533Phe
XM_006716590.3:c.13448C>T	XP_006716653.1:p.Ser4483Phe
XM_011517130.2:c.13517C>T	XP_011515432.1:p.Ser4506Phe
XM_011517131.2:c.13433C>T	XP_011515433.1:p.Ser4478Phe
XM_011517132.2:c.10148C>T	XP_011515434.1:p.Ser3383Phe
NM_000445.5:c.13583C>T	NP_000436.2:p.Ser4528Phe
NM_201378.4:c.13460C>T MANE Plus Clinical	NP_958780.1:p.Ser4487Phe
NM_201379.3:c.13436C>T	NP_958781.1:p.Ser4479Phe
NM_201380.4:c.13913C>T	NP_958782.1:p.Ser4638Phe
NM_201381.3:c.13406C>T	NP_958783.1:p.Ser4469Phe
NM_201382.4:c.13502C>T	NP_958784.1:p.Ser4501Phe
NM_201383.3:c.13514C>T	NP_958785.1:p.Ser4505Phe
NM_201384.3:c.13502C>T MANE Select	NP_958786.1:p.Ser4501Phe