Canonical Allele Identifier: CA463525890

Gene: PLEC

Linked Data

• gnomAD v4: 8-143916648-C-T
• MyVariant Identifiers: chr8:g.144990816C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143916648C>T , CM000670.2:g.143916648C>T	GRCh38
NC_000008.10:g.144990816C>T , CM000670.1:g.144990816C>T	GRCh37
NC_000008.9:g.145062804C>T	NCBI36
NG_012492.1:g.65098G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528025.6:c.13305G>A	ENSP00000437303.2:p.Gln4435=
ENST00000685198.1:c.13224G>A	ENSP00000510528.1:p.Gln4408=
ENST00000687971.1:c.12891G>A	ENSP00000510788.1:p.Gln4297=
ENST00000693060.1:c.13104G>A	ENSP00000510329.1:p.Gln4368=
ENST00000345136.8:c.13173G>A MANE Select	ENSP00000344848.3:p.Gln4391=
ENST00000527303.2:c.9873G>A	ENSP00000433982.2:p.Gln3291=
ENST00000322810.8:c.13584G>A	ENSP00000323856.4:p.Gln4528=
ENST00000345136.7:c.13173G>A	ENSP00000344848.3:p.Gln4391=
ENST00000354589.7:c.13173G>A	ENSP00000346602.3:p.Gln4391=
ENST00000354958.6:c.13107G>A	ENSP00000347044.2:p.Gln4369=
ENST00000356346.7:c.13131G>A MANE Plus Clinical	ENSP00000348702.3:p.Gln4377=
ENST00000357649.6:c.13185G>A	ENSP00000350277.2:p.Gln4395=
ENST00000398774.6:c.13077G>A	ENSP00000381756.2:p.Gln4359=
ENST00000436759.6:c.13254G>A	ENSP00000388180.2:p.Gln4418=
ENST00000527096.5:c.13242G>A	ENSP00000434583.1:p.Gln4414=
NM_000445.4:c.13254G>A	NP_000436.2:p.Gln4418=
NM_201378.3:c.13131G>A	NP_958780.1:p.Gln4377=
NM_201379.2:c.13107G>A	NP_958781.1:p.Gln4369=
NM_201380.3:c.13584G>A	NP_958782.1:p.Gln4528=
NM_201381.2:c.13077G>A	NP_958783.1:p.Gln4359=
NM_201382.3:c.13173G>A	NP_958784.1:p.Gln4391=
NM_201383.2:c.13185G>A	NP_958785.1:p.Gln4395=
NM_201384.2:c.13173G>A	NP_958786.1:p.Gln4391=
XM_005250976.2:c.13599G>A	XP_005251033.1:p.Gln4533=
XM_005250978.2:c.13200G>A	XP_005251035.1:p.Gln4400=
XM_005250979.3:c.13188G>A	XP_005251036.1:p.Gln4396=
XM_005250980.3:c.13188G>A	XP_005251037.1:p.Gln4396=
XM_005250981.2:c.13146G>A	XP_005251038.1:p.Gln4382=
XM_005250982.2:c.13122G>A	XP_005251039.1:p.Gln4374=
XM_005250983.2:c.13104G>A	XP_005251040.1:p.Gln4368=
XM_005250984.3:c.13092G>A	XP_005251041.1:p.Gln4364=
XM_006716588.2:c.13269G>A	XP_006716651.1:p.Gln4423=
XM_006716589.2:c.13119G>A	XP_006716652.1:p.Gln4373=
XM_006716590.2:c.13119G>A	XP_006716653.1:p.Gln4373=
XM_011517130.1:c.13188G>A	XP_011515432.1:p.Gln4396=
XM_011517131.1:c.13104G>A	XP_011515433.1:p.Gln4368=
XM_011517132.1:c.9819G>A	XP_011515434.1:p.Gln3273=
XM_005250976.4:c.13599G>A	XP_005251033.1:p.Gln4533=
XM_005250978.3:c.13200G>A	XP_005251035.1:p.Gln4400=
XM_005250979.4:c.13188G>A	XP_005251036.1:p.Gln4396=
XM_005250980.4:c.13188G>A	XP_005251037.1:p.Gln4396=
XM_005250981.3:c.13146G>A	XP_005251038.1:p.Gln4382=
XM_005250982.4:c.13122G>A	XP_005251039.1:p.Gln4374=
XM_005250984.5:c.13092G>A	XP_005251041.1:p.Gln4364=
XM_006716588.3:c.13269G>A	XP_006716651.1:p.Gln4423=
XM_006716590.3:c.13119G>A	XP_006716653.1:p.Gln4373=
XM_011517130.2:c.13188G>A	XP_011515432.1:p.Gln4396=
XM_011517131.2:c.13104G>A	XP_011515433.1:p.Gln4368=
XM_011517132.2:c.9819G>A	XP_011515434.1:p.Gln3273=
NM_000445.5:c.13254G>A	NP_000436.2:p.Gln4418=
NM_201378.4:c.13131G>A MANE Plus Clinical	NP_958780.1:p.Gln4377=
NM_201379.3:c.13107G>A	NP_958781.1:p.Gln4369=
NM_201380.4:c.13584G>A	NP_958782.1:p.Gln4528=
NM_201381.3:c.13077G>A	NP_958783.1:p.Gln4359=
NM_201382.4:c.13173G>A	NP_958784.1:p.Gln4391=
NM_201383.3:c.13185G>A	NP_958785.1:p.Gln4395=
NM_201384.3:c.13173G>A MANE Select	NP_958786.1:p.Gln4391=