Canonical Allele Identifier: CA187606024

Gene: PLEC

Linked Data

• dbSNP Id: rs960573896
• MyVariant Identifiers: chr8:g.144990494C>A (hg19) ; chr8:g.143916326C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143916326C>A , CM000670.2:g.143916326C>A	GRCh38
NC_000008.10:g.144990494C>A , CM000670.1:g.144990494C>A	GRCh37
NC_000008.9:g.145062482C>A	NCBI36
NG_012492.1:g.65420G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528025.6:c.13627G>T	ENSP00000437303.2:p.Ala4543Ser
ENST00000685198.1:c.13546G>T	ENSP00000510528.1:p.Ala4516Ser
ENST00000687971.1:c.13213G>T	ENSP00000510788.1:p.Ala4405Ser
ENST00000693060.1:c.13426G>T	ENSP00000510329.1:p.Ala4476Ser
ENST00000345136.8:c.13495G>T MANE Select	ENSP00000344848.3:p.Ala4499Ser
ENST00000527303.2:c.10195G>T	ENSP00000433982.2:p.Ala3399Ser
ENST00000322810.8:c.13906G>T	ENSP00000323856.4:p.Ala4636Ser
ENST00000345136.7:c.13495G>T	ENSP00000344848.3:p.Ala4499Ser
ENST00000354589.7:c.13495G>T	ENSP00000346602.3:p.Ala4499Ser
ENST00000354958.6:c.13429G>T	ENSP00000347044.2:p.Ala4477Ser
ENST00000356346.7:c.13453G>T MANE Plus Clinical	ENSP00000348702.3:p.Ala4485Ser
ENST00000357649.6:c.13507G>T	ENSP00000350277.2:p.Ala4503Ser
ENST00000398774.6:c.13399G>T	ENSP00000381756.2:p.Ala4467Ser
ENST00000436759.6:c.13576G>T	ENSP00000388180.2:p.Ala4526Ser
ENST00000527096.5:c.13564G>T	ENSP00000434583.1:p.Ala4522Ser
NM_000445.4:c.13576G>T	NP_000436.2:p.Ala4526Ser
NM_201378.3:c.13453G>T	NP_958780.1:p.Ala4485Ser
NM_201379.2:c.13429G>T	NP_958781.1:p.Ala4477Ser
NM_201380.3:c.13906G>T	NP_958782.1:p.Ala4636Ser
NM_201381.2:c.13399G>T	NP_958783.1:p.Ala4467Ser
NM_201382.3:c.13495G>T	NP_958784.1:p.Ala4499Ser
NM_201383.2:c.13507G>T	NP_958785.1:p.Ala4503Ser
NM_201384.2:c.13495G>T	NP_958786.1:p.Ala4499Ser
XM_005250976.2:c.13921G>T	XP_005251033.1:p.Ala4641Ser
XM_005250978.2:c.13522G>T	XP_005251035.1:p.Ala4508Ser
XM_005250979.3:c.13510G>T	XP_005251036.1:p.Ala4504Ser
XM_005250980.3:c.13510G>T	XP_005251037.1:p.Ala4504Ser
XM_005250981.2:c.13468G>T	XP_005251038.1:p.Ala4490Ser
XM_005250982.2:c.13444G>T	XP_005251039.1:p.Ala4482Ser
XM_005250983.2:c.13426G>T	XP_005251040.1:p.Ala4476Ser
XM_005250984.3:c.13414G>T	XP_005251041.1:p.Ala4472Ser
XM_006716588.2:c.13591G>T	XP_006716651.1:p.Ala4531Ser
XM_006716589.2:c.13441G>T	XP_006716652.1:p.Ala4481Ser
XM_006716590.2:c.13441G>T	XP_006716653.1:p.Ala4481Ser
XM_011517130.1:c.13510G>T	XP_011515432.1:p.Ala4504Ser
XM_011517131.1:c.13426G>T	XP_011515433.1:p.Ala4476Ser
XM_011517132.1:c.10141G>T	XP_011515434.1:p.Ala3381Ser
XM_005250976.4:c.13921G>T	XP_005251033.1:p.Ala4641Ser
XM_005250978.3:c.13522G>T	XP_005251035.1:p.Ala4508Ser
XM_005250979.4:c.13510G>T	XP_005251036.1:p.Ala4504Ser
XM_005250980.4:c.13510G>T	XP_005251037.1:p.Ala4504Ser
XM_005250981.3:c.13468G>T	XP_005251038.1:p.Ala4490Ser
XM_005250982.4:c.13444G>T	XP_005251039.1:p.Ala4482Ser
XM_005250984.5:c.13414G>T	XP_005251041.1:p.Ala4472Ser
XM_006716588.3:c.13591G>T	XP_006716651.1:p.Ala4531Ser
XM_006716590.3:c.13441G>T	XP_006716653.1:p.Ala4481Ser
XM_011517130.2:c.13510G>T	XP_011515432.1:p.Ala4504Ser
XM_011517131.2:c.13426G>T	XP_011515433.1:p.Ala4476Ser
XM_011517132.2:c.10141G>T	XP_011515434.1:p.Ala3381Ser
NM_000445.5:c.13576G>T	NP_000436.2:p.Ala4526Ser
NM_201378.4:c.13453G>T MANE Plus Clinical	NP_958780.1:p.Ala4485Ser
NM_201379.3:c.13429G>T	NP_958781.1:p.Ala4477Ser
NM_201380.4:c.13906G>T	NP_958782.1:p.Ala4636Ser
NM_201381.3:c.13399G>T	NP_958783.1:p.Ala4467Ser
NM_201382.4:c.13495G>T	NP_958784.1:p.Ala4499Ser
NM_201383.3:c.13507G>T	NP_958785.1:p.Ala4503Ser
NM_201384.3:c.13495G>T MANE Select	NP_958786.1:p.Ala4499Ser