Canonical Allele Identifier: CA372475641

Gene: PLEC

Linked Data

• MyVariant Identifiers: chr8:g.144990664A>T (hg19) ; chr8:g.143916496A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143916496A>T , CM000670.2:g.143916496A>T	GRCh38
NC_000008.10:g.144990664A>T , CM000670.1:g.144990664A>T	GRCh37
NC_000008.9:g.145062652A>T	NCBI36
NG_012492.1:g.65250T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528025.6:c.13457T>A	ENSP00000437303.2:p.Leu4486His
ENST00000685198.1:c.13376T>A	ENSP00000510528.1:p.Leu4459His
ENST00000687971.1:c.13043T>A	ENSP00000510788.1:p.Leu4348His
ENST00000693060.1:c.13256T>A	ENSP00000510329.1:p.Leu4419His
ENST00000345136.8:c.13325T>A MANE Select	ENSP00000344848.3:p.Leu4442His
ENST00000527303.2:c.10025T>A	ENSP00000433982.2:p.Leu3342His
ENST00000322810.8:c.13736T>A	ENSP00000323856.4:p.Leu4579His
ENST00000345136.7:c.13325T>A	ENSP00000344848.3:p.Leu4442His
ENST00000354589.7:c.13325T>A	ENSP00000346602.3:p.Leu4442His
ENST00000354958.6:c.13259T>A	ENSP00000347044.2:p.Leu4420His
ENST00000356346.7:c.13283T>A MANE Plus Clinical	ENSP00000348702.3:p.Leu4428His
ENST00000357649.6:c.13337T>A	ENSP00000350277.2:p.Leu4446His
ENST00000398774.6:c.13229T>A	ENSP00000381756.2:p.Leu4410His
ENST00000436759.6:c.13406T>A	ENSP00000388180.2:p.Leu4469His
ENST00000527096.5:c.13394T>A	ENSP00000434583.1:p.Leu4465His
NM_000445.4:c.13406T>A	NP_000436.2:p.Leu4469His
NM_201378.3:c.13283T>A	NP_958780.1:p.Leu4428His
NM_201379.2:c.13259T>A	NP_958781.1:p.Leu4420His
NM_201380.3:c.13736T>A	NP_958782.1:p.Leu4579His
NM_201381.2:c.13229T>A	NP_958783.1:p.Leu4410His
NM_201382.3:c.13325T>A	NP_958784.1:p.Leu4442His
NM_201383.2:c.13337T>A	NP_958785.1:p.Leu4446His
NM_201384.2:c.13325T>A	NP_958786.1:p.Leu4442His
XM_005250976.2:c.13751T>A	XP_005251033.1:p.Leu4584His
XM_005250978.2:c.13352T>A	XP_005251035.1:p.Leu4451His
XM_005250979.3:c.13340T>A	XP_005251036.1:p.Leu4447His
XM_005250980.3:c.13340T>A	XP_005251037.1:p.Leu4447His
XM_005250981.2:c.13298T>A	XP_005251038.1:p.Leu4433His
XM_005250982.2:c.13274T>A	XP_005251039.1:p.Leu4425His
XM_005250983.2:c.13256T>A	XP_005251040.1:p.Leu4419His
XM_005250984.3:c.13244T>A	XP_005251041.1:p.Leu4415His
XM_006716588.2:c.13421T>A	XP_006716651.1:p.Leu4474His
XM_006716589.2:c.13271T>A	XP_006716652.1:p.Leu4424His
XM_006716590.2:c.13271T>A	XP_006716653.1:p.Leu4424His
XM_011517130.1:c.13340T>A	XP_011515432.1:p.Leu4447His
XM_011517131.1:c.13256T>A	XP_011515433.1:p.Leu4419His
XM_011517132.1:c.9971T>A	XP_011515434.1:p.Leu3324His
XM_005250976.4:c.13751T>A	XP_005251033.1:p.Leu4584His
XM_005250978.3:c.13352T>A	XP_005251035.1:p.Leu4451His
XM_005250979.4:c.13340T>A	XP_005251036.1:p.Leu4447His
XM_005250980.4:c.13340T>A	XP_005251037.1:p.Leu4447His
XM_005250981.3:c.13298T>A	XP_005251038.1:p.Leu4433His
XM_005250982.4:c.13274T>A	XP_005251039.1:p.Leu4425His
XM_005250984.5:c.13244T>A	XP_005251041.1:p.Leu4415His
XM_006716588.3:c.13421T>A	XP_006716651.1:p.Leu4474His
XM_006716590.3:c.13271T>A	XP_006716653.1:p.Leu4424His
XM_011517130.2:c.13340T>A	XP_011515432.1:p.Leu4447His
XM_011517131.2:c.13256T>A	XP_011515433.1:p.Leu4419His
XM_011517132.2:c.9971T>A	XP_011515434.1:p.Leu3324His
NM_000445.5:c.13406T>A	NP_000436.2:p.Leu4469His
NM_201378.4:c.13283T>A MANE Plus Clinical	NP_958780.1:p.Leu4428His
NM_201379.3:c.13259T>A	NP_958781.1:p.Leu4420His
NM_201380.4:c.13736T>A	NP_958782.1:p.Leu4579His
NM_201381.3:c.13229T>A	NP_958783.1:p.Leu4410His
NM_201382.4:c.13325T>A	NP_958784.1:p.Leu4442His
NM_201383.3:c.13337T>A	NP_958785.1:p.Leu4446His
NM_201384.3:c.13325T>A MANE Select	NP_958786.1:p.Leu4442His