Canonical Allele Identifier: CA372474616

Gene: PLEC

Linked Data

• dbSNP Id: rs1820573235
• MyVariant Identifiers: chr8:g.144990589G>C (hg19) ; chr8:g.143916421G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143916421G>C , CM000670.2:g.143916421G>C	GRCh38
NC_000008.10:g.144990589G>C , CM000670.1:g.144990589G>C	GRCh37
NC_000008.9:g.145062577G>C	NCBI36
NG_012492.1:g.65325C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528025.6:c.13532C>G	ENSP00000437303.2:p.Ala4511Gly
ENST00000685198.1:c.13451C>G	ENSP00000510528.1:p.Ala4484Gly
ENST00000687971.1:c.13118C>G	ENSP00000510788.1:p.Ala4373Gly
ENST00000693060.1:c.13331C>G	ENSP00000510329.1:p.Ala4444Gly
ENST00000345136.8:c.13400C>G MANE Select	ENSP00000344848.3:p.Ala4467Gly
ENST00000527303.2:c.10100C>G	ENSP00000433982.2:p.Ala3367Gly
ENST00000322810.8:c.13811C>G	ENSP00000323856.4:p.Ala4604Gly
ENST00000345136.7:c.13400C>G	ENSP00000344848.3:p.Ala4467Gly
ENST00000354589.7:c.13400C>G	ENSP00000346602.3:p.Ala4467Gly
ENST00000354958.6:c.13334C>G	ENSP00000347044.2:p.Ala4445Gly
ENST00000356346.7:c.13358C>G MANE Plus Clinical	ENSP00000348702.3:p.Ala4453Gly
ENST00000357649.6:c.13412C>G	ENSP00000350277.2:p.Ala4471Gly
ENST00000398774.6:c.13304C>G	ENSP00000381756.2:p.Ala4435Gly
ENST00000436759.6:c.13481C>G	ENSP00000388180.2:p.Ala4494Gly
ENST00000527096.5:c.13469C>G	ENSP00000434583.1:p.Ala4490Gly
NM_000445.4:c.13481C>G	NP_000436.2:p.Ala4494Gly
NM_201378.3:c.13358C>G	NP_958780.1:p.Ala4453Gly
NM_201379.2:c.13334C>G	NP_958781.1:p.Ala4445Gly
NM_201380.3:c.13811C>G	NP_958782.1:p.Ala4604Gly
NM_201381.2:c.13304C>G	NP_958783.1:p.Ala4435Gly
NM_201382.3:c.13400C>G	NP_958784.1:p.Ala4467Gly
NM_201383.2:c.13412C>G	NP_958785.1:p.Ala4471Gly
NM_201384.2:c.13400C>G	NP_958786.1:p.Ala4467Gly
XM_005250976.2:c.13826C>G	XP_005251033.1:p.Ala4609Gly
XM_005250978.2:c.13427C>G	XP_005251035.1:p.Ala4476Gly
XM_005250979.3:c.13415C>G	XP_005251036.1:p.Ala4472Gly
XM_005250980.3:c.13415C>G	XP_005251037.1:p.Ala4472Gly
XM_005250981.2:c.13373C>G	XP_005251038.1:p.Ala4458Gly
XM_005250982.2:c.13349C>G	XP_005251039.1:p.Ala4450Gly
XM_005250983.2:c.13331C>G	XP_005251040.1:p.Ala4444Gly
XM_005250984.3:c.13319C>G	XP_005251041.1:p.Ala4440Gly
XM_006716588.2:c.13496C>G	XP_006716651.1:p.Ala4499Gly
XM_006716589.2:c.13346C>G	XP_006716652.1:p.Ala4449Gly
XM_006716590.2:c.13346C>G	XP_006716653.1:p.Ala4449Gly
XM_011517130.1:c.13415C>G	XP_011515432.1:p.Ala4472Gly
XM_011517131.1:c.13331C>G	XP_011515433.1:p.Ala4444Gly
XM_011517132.1:c.10046C>G	XP_011515434.1:p.Ala3349Gly
XM_005250976.4:c.13826C>G	XP_005251033.1:p.Ala4609Gly
XM_005250978.3:c.13427C>G	XP_005251035.1:p.Ala4476Gly
XM_005250979.4:c.13415C>G	XP_005251036.1:p.Ala4472Gly
XM_005250980.4:c.13415C>G	XP_005251037.1:p.Ala4472Gly
XM_005250981.3:c.13373C>G	XP_005251038.1:p.Ala4458Gly
XM_005250982.4:c.13349C>G	XP_005251039.1:p.Ala4450Gly
XM_005250984.5:c.13319C>G	XP_005251041.1:p.Ala4440Gly
XM_006716588.3:c.13496C>G	XP_006716651.1:p.Ala4499Gly
XM_006716590.3:c.13346C>G	XP_006716653.1:p.Ala4449Gly
XM_011517130.2:c.13415C>G	XP_011515432.1:p.Ala4472Gly
XM_011517131.2:c.13331C>G	XP_011515433.1:p.Ala4444Gly
XM_011517132.2:c.10046C>G	XP_011515434.1:p.Ala3349Gly
NM_000445.5:c.13481C>G	NP_000436.2:p.Ala4494Gly
NM_201378.4:c.13358C>G MANE Plus Clinical	NP_958780.1:p.Ala4453Gly
NM_201379.3:c.13334C>G	NP_958781.1:p.Ala4445Gly
NM_201380.4:c.13811C>G	NP_958782.1:p.Ala4604Gly
NM_201381.3:c.13304C>G	NP_958783.1:p.Ala4435Gly
NM_201382.4:c.13400C>G	NP_958784.1:p.Ala4467Gly
NM_201383.3:c.13412C>G	NP_958785.1:p.Ala4471Gly
NM_201384.3:c.13400C>G MANE Select	NP_958786.1:p.Ala4467Gly