Canonical Allele Identifier: CA372586856

Gene: PLEC

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143934930C>T , CM000670.2:g.143934930C>T	GRCh38
NC_000008.10:g.145009098C>T , CM000670.1:g.145009098C>T	GRCh37
NC_000008.9:g.145081086C>T	NCBI36
NG_012492.1:g.46816G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_201384.3:c.826-1G>A MANE Select	NP_958786.1:n.826-1G>A
ENST00000345136.8:c.826-1G>A MANE Select	ENSP00000344848.3:n.826-1G>A
NM_201378.4:c.784-1G>A MANE Plus Clinical	NP_958780.1:n.784-1G>A
ENST00000356346.7:c.784-1G>A MANE Plus Clinical	ENSP00000348702.3:n.784-1G>A
NM_000445.4:c.907-1G>A	NP_000436.2:n.907-1G>A
NM_000445.5:c.907-1G>A	NP_000436.2:n.907-1G>A
NM_201378.3:c.784-1G>A	NP_958780.1:n.784-1G>A
NM_201379.2:c.760-1G>A	NP_958781.1:n.760-1G>A
NM_201379.3:c.760-1G>A	NP_958781.1:n.760-1G>A
NM_201380.3:c.1237-1G>A	NP_958782.1:n.1237-1G>A
NM_201380.4:c.1237-1G>A	NP_958782.1:n.1237-1G>A
NM_201381.2:c.730-1G>A	NP_958783.1:n.730-1G>A
NM_201381.3:c.730-1G>A	NP_958783.1:n.730-1G>A
NM_201382.3:c.826-1G>A	NP_958784.1:n.826-1G>A
NM_201382.4:c.826-1G>A	NP_958784.1:n.826-1G>A
NM_201383.2:c.838-1G>A	NP_958785.1:n.838-1G>A
NM_201383.3:c.838-1G>A	NP_958785.1:n.838-1G>A
NM_201384.2:c.826-1G>A	NP_958786.1:n.826-1G>A
ENST00000322810.8:c.1237-1G>A	ENSP00000323856.4:n.1237-1G>A
ENST00000345136.7:c.826-1G>A	ENSP00000344848.3:n.826-1G>A
ENST00000354589.7:c.826-1G>A	ENSP00000346602.3:n.826-1G>A
ENST00000354958.6:c.760-1G>A	ENSP00000347044.2:n.760-1G>A
ENST00000357649.6:c.838-1G>A	ENSP00000350277.2:n.838-1G>A
ENST00000398774.6:c.730-1G>A	ENSP00000381756.2:n.730-1G>A
ENST00000436759.6:c.907-1G>A	ENSP00000388180.2:n.907-1G>A
ENST00000527096.5:c.895-1G>A	ENSP00000434583.1:n.895-1G>A
ENST00000527303.2:c.907-1G>A	ENSP00000433982.2:n.907-1G>A
ENST00000528025.5:c.958-1G>A	ENSP00000437303.1:n.958-1G>A
ENST00000528025.6:c.958-1G>A	ENSP00000437303.2:n.958-1G>A
ENST00000685198.1:c.877-1G>A	ENSP00000510528.1:n.877-1G>A
ENST00000687971.1:c.544-1G>A	ENSP00000510788.1:n.544-1G>A
ENST00000693060.1:c.757-1G>A	ENSP00000510329.1:n.757-1G>A
XM_005250976.2:c.1252-1G>A	XP_005251033.1:n.1252-1G>A
XM_005250976.4:c.1252-1G>A	XP_005251033.1:n.1252-1G>A
XM_005250978.2:c.853-1G>A	XP_005251035.1:n.853-1G>A
XM_005250978.3:c.853-1G>A	XP_005251035.1:n.853-1G>A
XM_005250979.3:c.841-1G>A	XP_005251036.1:n.841-1G>A
XM_005250979.4:c.841-1G>A	XP_005251036.1:n.841-1G>A
XM_005250980.3:c.841-1G>A	XP_005251037.1:n.841-1G>A
XM_005250980.4:c.841-1G>A	XP_005251037.1:n.841-1G>A
XM_005250981.2:c.799-1G>A	XP_005251038.1:n.799-1G>A
XM_005250981.3:c.799-1G>A	XP_005251038.1:n.799-1G>A
XM_005250982.2:c.775-1G>A	XP_005251039.1:n.775-1G>A
XM_005250982.4:c.775-1G>A	XP_005251039.1:n.775-1G>A
XM_005250983.2:c.757-1G>A	XP_005251040.1:n.757-1G>A
XM_005250984.3:c.745-1G>A	XP_005251041.1:n.745-1G>A
XM_005250984.5:c.745-1G>A	XP_005251041.1:n.745-1G>A
XM_006716588.2:c.922-1G>A	XP_006716651.1:n.922-1G>A
XM_006716588.3:c.922-1G>A	XP_006716651.1:n.922-1G>A
XM_006716589.2:c.772-1G>A	XP_006716652.1:n.772-1G>A
XM_006716590.2:c.772-1G>A	XP_006716653.1:n.772-1G>A
XM_006716590.3:c.772-1G>A	XP_006716653.1:n.772-1G>A
XM_011517130.1:c.841-1G>A	XP_011515432.1:n.841-1G>A
XM_011517130.2:c.841-1G>A	XP_011515432.1:n.841-1G>A
XM_011517131.1:c.757-1G>A	XP_011515433.1:n.757-1G>A
XM_011517131.2:c.757-1G>A	XP_011515433.1:n.757-1G>A
XM_011517132.1:c.853-1G>A	XP_011515434.1:n.853-1G>A
XM_011517132.2:c.853-1G>A	XP_011515434.1:n.853-1G>A