Canonical Allele Identifier: CA372476063

Gene: PLEC

Linked Data

• MyVariant Identifiers: chr8:g.144990799A>G (hg19) ; chr8:g.143916631A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143916631A>G , CM000670.2:g.143916631A>G	GRCh38
NC_000008.10:g.144990799A>G , CM000670.1:g.144990799A>G	GRCh37
NC_000008.9:g.145062787A>G	NCBI36
NG_012492.1:g.65115T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528025.6:c.13322T>C	ENSP00000437303.2:p.Leu4441Ser
ENST00000685198.1:c.13241T>C	ENSP00000510528.1:p.Leu4414Ser
ENST00000687971.1:c.12908T>C	ENSP00000510788.1:p.Leu4303Ser
ENST00000693060.1:c.13121T>C	ENSP00000510329.1:p.Leu4374Ser
ENST00000345136.8:c.13190T>C MANE Select	ENSP00000344848.3:p.Leu4397Ser
ENST00000527303.2:c.9890T>C	ENSP00000433982.2:p.Leu3297Ser
ENST00000322810.8:c.13601T>C	ENSP00000323856.4:p.Leu4534Ser
ENST00000345136.7:c.13190T>C	ENSP00000344848.3:p.Leu4397Ser
ENST00000354589.7:c.13190T>C	ENSP00000346602.3:p.Leu4397Ser
ENST00000354958.6:c.13124T>C	ENSP00000347044.2:p.Leu4375Ser
ENST00000356346.7:c.13148T>C MANE Plus Clinical	ENSP00000348702.3:p.Leu4383Ser
ENST00000357649.6:c.13202T>C	ENSP00000350277.2:p.Leu4401Ser
ENST00000398774.6:c.13094T>C	ENSP00000381756.2:p.Leu4365Ser
ENST00000436759.6:c.13271T>C	ENSP00000388180.2:p.Leu4424Ser
ENST00000527096.5:c.13259T>C	ENSP00000434583.1:p.Leu4420Ser
NM_000445.4:c.13271T>C	NP_000436.2:p.Leu4424Ser
NM_201378.3:c.13148T>C	NP_958780.1:p.Leu4383Ser
NM_201379.2:c.13124T>C	NP_958781.1:p.Leu4375Ser
NM_201380.3:c.13601T>C	NP_958782.1:p.Leu4534Ser
NM_201381.2:c.13094T>C	NP_958783.1:p.Leu4365Ser
NM_201382.3:c.13190T>C	NP_958784.1:p.Leu4397Ser
NM_201383.2:c.13202T>C	NP_958785.1:p.Leu4401Ser
NM_201384.2:c.13190T>C	NP_958786.1:p.Leu4397Ser
XM_005250976.2:c.13616T>C	XP_005251033.1:p.Leu4539Ser
XM_005250978.2:c.13217T>C	XP_005251035.1:p.Leu4406Ser
XM_005250979.3:c.13205T>C	XP_005251036.1:p.Leu4402Ser
XM_005250980.3:c.13205T>C	XP_005251037.1:p.Leu4402Ser
XM_005250981.2:c.13163T>C	XP_005251038.1:p.Leu4388Ser
XM_005250982.2:c.13139T>C	XP_005251039.1:p.Leu4380Ser
XM_005250983.2:c.13121T>C	XP_005251040.1:p.Leu4374Ser
XM_005250984.3:c.13109T>C	XP_005251041.1:p.Leu4370Ser
XM_006716588.2:c.13286T>C	XP_006716651.1:p.Leu4429Ser
XM_006716589.2:c.13136T>C	XP_006716652.1:p.Leu4379Ser
XM_006716590.2:c.13136T>C	XP_006716653.1:p.Leu4379Ser
XM_011517130.1:c.13205T>C	XP_011515432.1:p.Leu4402Ser
XM_011517131.1:c.13121T>C	XP_011515433.1:p.Leu4374Ser
XM_011517132.1:c.9836T>C	XP_011515434.1:p.Leu3279Ser
XM_005250976.4:c.13616T>C	XP_005251033.1:p.Leu4539Ser
XM_005250978.3:c.13217T>C	XP_005251035.1:p.Leu4406Ser
XM_005250979.4:c.13205T>C	XP_005251036.1:p.Leu4402Ser
XM_005250980.4:c.13205T>C	XP_005251037.1:p.Leu4402Ser
XM_005250981.3:c.13163T>C	XP_005251038.1:p.Leu4388Ser
XM_005250982.4:c.13139T>C	XP_005251039.1:p.Leu4380Ser
XM_005250984.5:c.13109T>C	XP_005251041.1:p.Leu4370Ser
XM_006716588.3:c.13286T>C	XP_006716651.1:p.Leu4429Ser
XM_006716590.3:c.13136T>C	XP_006716653.1:p.Leu4379Ser
XM_011517130.2:c.13205T>C	XP_011515432.1:p.Leu4402Ser
XM_011517131.2:c.13121T>C	XP_011515433.1:p.Leu4374Ser
XM_011517132.2:c.9836T>C	XP_011515434.1:p.Leu3279Ser
NM_000445.5:c.13271T>C	NP_000436.2:p.Leu4424Ser
NM_201378.4:c.13148T>C MANE Plus Clinical	NP_958780.1:p.Leu4383Ser
NM_201379.3:c.13124T>C	NP_958781.1:p.Leu4375Ser
NM_201380.4:c.13601T>C	NP_958782.1:p.Leu4534Ser
NM_201381.3:c.13094T>C	NP_958783.1:p.Leu4365Ser
NM_201382.4:c.13190T>C	NP_958784.1:p.Leu4397Ser
NM_201383.3:c.13202T>C	NP_958785.1:p.Leu4401Ser
NM_201384.3:c.13190T>C MANE Select	NP_958786.1:p.Leu4397Ser