Canonical Allele Identifier: CA372475718

Gene: PLEC

Linked Data

• gnomAD v4: 8-143916532-G-A
• MyVariant Identifiers: chr8:g.144990700G>A (hg19) ; chr8:g.143916532G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143916532G>A , CM000670.2:g.143916532G>A	GRCh38
NC_000008.10:g.144990700G>A , CM000670.1:g.144990700G>A	GRCh37
NC_000008.9:g.145062688G>A	NCBI36
NG_012492.1:g.65214C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528025.6:c.13421C>T	ENSP00000437303.2:p.Ala4474Val
ENST00000685198.1:c.13340C>T	ENSP00000510528.1:p.Ala4447Val
ENST00000687971.1:c.13007C>T	ENSP00000510788.1:p.Ala4336Val
ENST00000693060.1:c.13220C>T	ENSP00000510329.1:p.Ala4407Val
ENST00000345136.8:c.13289C>T MANE Select	ENSP00000344848.3:p.Ala4430Val
ENST00000527303.2:c.9989C>T	ENSP00000433982.2:p.Ala3330Val
ENST00000322810.8:c.13700C>T	ENSP00000323856.4:p.Ala4567Val
ENST00000345136.7:c.13289C>T	ENSP00000344848.3:p.Ala4430Val
ENST00000354589.7:c.13289C>T	ENSP00000346602.3:p.Ala4430Val
ENST00000354958.6:c.13223C>T	ENSP00000347044.2:p.Ala4408Val
ENST00000356346.7:c.13247C>T MANE Plus Clinical	ENSP00000348702.3:p.Ala4416Val
ENST00000357649.6:c.13301C>T	ENSP00000350277.2:p.Ala4434Val
ENST00000398774.6:c.13193C>T	ENSP00000381756.2:p.Ala4398Val
ENST00000436759.6:c.13370C>T	ENSP00000388180.2:p.Ala4457Val
ENST00000527096.5:c.13358C>T	ENSP00000434583.1:p.Ala4453Val
NM_000445.4:c.13370C>T	NP_000436.2:p.Ala4457Val
NM_201378.3:c.13247C>T	NP_958780.1:p.Ala4416Val
NM_201379.2:c.13223C>T	NP_958781.1:p.Ala4408Val
NM_201380.3:c.13700C>T	NP_958782.1:p.Ala4567Val
NM_201381.2:c.13193C>T	NP_958783.1:p.Ala4398Val
NM_201382.3:c.13289C>T	NP_958784.1:p.Ala4430Val
NM_201383.2:c.13301C>T	NP_958785.1:p.Ala4434Val
NM_201384.2:c.13289C>T	NP_958786.1:p.Ala4430Val
XM_005250976.2:c.13715C>T	XP_005251033.1:p.Ala4572Val
XM_005250978.2:c.13316C>T	XP_005251035.1:p.Ala4439Val
XM_005250979.3:c.13304C>T	XP_005251036.1:p.Ala4435Val
XM_005250980.3:c.13304C>T	XP_005251037.1:p.Ala4435Val
XM_005250981.2:c.13262C>T	XP_005251038.1:p.Ala4421Val
XM_005250982.2:c.13238C>T	XP_005251039.1:p.Ala4413Val
XM_005250983.2:c.13220C>T	XP_005251040.1:p.Ala4407Val
XM_005250984.3:c.13208C>T	XP_005251041.1:p.Ala4403Val
XM_006716588.2:c.13385C>T	XP_006716651.1:p.Ala4462Val
XM_006716589.2:c.13235C>T	XP_006716652.1:p.Ala4412Val
XM_006716590.2:c.13235C>T	XP_006716653.1:p.Ala4412Val
XM_011517130.1:c.13304C>T	XP_011515432.1:p.Ala4435Val
XM_011517131.1:c.13220C>T	XP_011515433.1:p.Ala4407Val
XM_011517132.1:c.9935C>T	XP_011515434.1:p.Ala3312Val
XM_005250976.4:c.13715C>T	XP_005251033.1:p.Ala4572Val
XM_005250978.3:c.13316C>T	XP_005251035.1:p.Ala4439Val
XM_005250979.4:c.13304C>T	XP_005251036.1:p.Ala4435Val
XM_005250980.4:c.13304C>T	XP_005251037.1:p.Ala4435Val
XM_005250981.3:c.13262C>T	XP_005251038.1:p.Ala4421Val
XM_005250982.4:c.13238C>T	XP_005251039.1:p.Ala4413Val
XM_005250984.5:c.13208C>T	XP_005251041.1:p.Ala4403Val
XM_006716588.3:c.13385C>T	XP_006716651.1:p.Ala4462Val
XM_006716590.3:c.13235C>T	XP_006716653.1:p.Ala4412Val
XM_011517130.2:c.13304C>T	XP_011515432.1:p.Ala4435Val
XM_011517131.2:c.13220C>T	XP_011515433.1:p.Ala4407Val
XM_011517132.2:c.9935C>T	XP_011515434.1:p.Ala3312Val
NM_000445.5:c.13370C>T	NP_000436.2:p.Ala4457Val
NM_201378.4:c.13247C>T MANE Plus Clinical	NP_958780.1:p.Ala4416Val
NM_201379.3:c.13223C>T	NP_958781.1:p.Ala4408Val
NM_201380.4:c.13700C>T	NP_958782.1:p.Ala4567Val
NM_201381.3:c.13193C>T	NP_958783.1:p.Ala4398Val
NM_201382.4:c.13289C>T	NP_958784.1:p.Ala4430Val
NM_201383.3:c.13301C>T	NP_958785.1:p.Ala4434Val
NM_201384.3:c.13289C>T MANE Select	NP_958786.1:p.Ala4430Val