Canonical Allele Identifier: CA372475907

Gene: PLEC

Linked Data

• MyVariant Identifiers: chr8:g.144990761C>A (hg19) ; chr8:g.143916593C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143916593C>A , CM000670.2:g.143916593C>A	GRCh38
NC_000008.10:g.144990761C>A , CM000670.1:g.144990761C>A	GRCh37
NC_000008.9:g.145062749C>A	NCBI36
NG_012492.1:g.65153G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528025.6:c.13360G>T	ENSP00000437303.2:p.Glu4454Ter
ENST00000685198.1:c.13279G>T	ENSP00000510528.1:p.Glu4427Ter
ENST00000687971.1:c.12946G>T	ENSP00000510788.1:p.Glu4316Ter
ENST00000693060.1:c.13159G>T	ENSP00000510329.1:p.Glu4387Ter
ENST00000345136.8:c.13228G>T MANE Select	ENSP00000344848.3:p.Glu4410Ter
ENST00000527303.2:c.9928G>T	ENSP00000433982.2:p.Glu3310Ter
ENST00000322810.8:c.13639G>T	ENSP00000323856.4:p.Glu4547Ter
ENST00000345136.7:c.13228G>T	ENSP00000344848.3:p.Glu4410Ter
ENST00000354589.7:c.13228G>T	ENSP00000346602.3:p.Glu4410Ter
ENST00000354958.6:c.13162G>T	ENSP00000347044.2:p.Glu4388Ter
ENST00000356346.7:c.13186G>T MANE Plus Clinical	ENSP00000348702.3:p.Glu4396Ter
ENST00000357649.6:c.13240G>T	ENSP00000350277.2:p.Glu4414Ter
ENST00000398774.6:c.13132G>T	ENSP00000381756.2:p.Glu4378Ter
ENST00000436759.6:c.13309G>T	ENSP00000388180.2:p.Glu4437Ter
ENST00000527096.5:c.13297G>T	ENSP00000434583.1:p.Glu4433Ter
NM_000445.4:c.13309G>T	NP_000436.2:p.Glu4437Ter
NM_201378.3:c.13186G>T	NP_958780.1:p.Glu4396Ter
NM_201379.2:c.13162G>T	NP_958781.1:p.Glu4388Ter
NM_201380.3:c.13639G>T	NP_958782.1:p.Glu4547Ter
NM_201381.2:c.13132G>T	NP_958783.1:p.Glu4378Ter
NM_201382.3:c.13228G>T	NP_958784.1:p.Glu4410Ter
NM_201383.2:c.13240G>T	NP_958785.1:p.Glu4414Ter
NM_201384.2:c.13228G>T	NP_958786.1:p.Glu4410Ter
XM_005250976.2:c.13654G>T	XP_005251033.1:p.Glu4552Ter
XM_005250978.2:c.13255G>T	XP_005251035.1:p.Glu4419Ter
XM_005250979.3:c.13243G>T	XP_005251036.1:p.Glu4415Ter
XM_005250980.3:c.13243G>T	XP_005251037.1:p.Glu4415Ter
XM_005250981.2:c.13201G>T	XP_005251038.1:p.Glu4401Ter
XM_005250982.2:c.13177G>T	XP_005251039.1:p.Glu4393Ter
XM_005250983.2:c.13159G>T	XP_005251040.1:p.Glu4387Ter
XM_005250984.3:c.13147G>T	XP_005251041.1:p.Glu4383Ter
XM_006716588.2:c.13324G>T	XP_006716651.1:p.Glu4442Ter
XM_006716589.2:c.13174G>T	XP_006716652.1:p.Glu4392Ter
XM_006716590.2:c.13174G>T	XP_006716653.1:p.Glu4392Ter
XM_011517130.1:c.13243G>T	XP_011515432.1:p.Glu4415Ter
XM_011517131.1:c.13159G>T	XP_011515433.1:p.Glu4387Ter
XM_011517132.1:c.9874G>T	XP_011515434.1:p.Glu3292Ter
XM_005250976.4:c.13654G>T	XP_005251033.1:p.Glu4552Ter
XM_005250978.3:c.13255G>T	XP_005251035.1:p.Glu4419Ter
XM_005250979.4:c.13243G>T	XP_005251036.1:p.Glu4415Ter
XM_005250980.4:c.13243G>T	XP_005251037.1:p.Glu4415Ter
XM_005250981.3:c.13201G>T	XP_005251038.1:p.Glu4401Ter
XM_005250982.4:c.13177G>T	XP_005251039.1:p.Glu4393Ter
XM_005250984.5:c.13147G>T	XP_005251041.1:p.Glu4383Ter
XM_006716588.3:c.13324G>T	XP_006716651.1:p.Glu4442Ter
XM_006716590.3:c.13174G>T	XP_006716653.1:p.Glu4392Ter
XM_011517130.2:c.13243G>T	XP_011515432.1:p.Glu4415Ter
XM_011517131.2:c.13159G>T	XP_011515433.1:p.Glu4387Ter
XM_011517132.2:c.9874G>T	XP_011515434.1:p.Glu3292Ter
NM_000445.5:c.13309G>T	NP_000436.2:p.Glu4437Ter
NM_201378.4:c.13186G>T MANE Plus Clinical	NP_958780.1:p.Glu4396Ter
NM_201379.3:c.13162G>T	NP_958781.1:p.Glu4388Ter
NM_201380.4:c.13639G>T	NP_958782.1:p.Glu4547Ter
NM_201381.3:c.13132G>T	NP_958783.1:p.Glu4378Ter
NM_201382.4:c.13228G>T	NP_958784.1:p.Glu4410Ter
NM_201383.3:c.13240G>T	NP_958785.1:p.Glu4414Ter
NM_201384.3:c.13228G>T MANE Select	NP_958786.1:p.Glu4410Ter