Canonical Allele Identifier: CA372573749

Gene: PLEC

Linked Data

• dbSNP Id: rs2131764927
• MyVariant Identifiers: chr8:g.145004337G>A (hg19) ; chr8:g.143930169G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143930169G>A , CM000670.2:g.143930169G>A	GRCh38
NC_000008.10:g.145004337G>A , CM000670.1:g.145004337G>A	GRCh37
NC_000008.9:g.145076325G>A	NCBI36
NG_012492.1:g.51577C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528025.6:c.2719C>T	ENSP00000437303.2:p.Gln907Ter
ENST00000685198.1:c.2638C>T	ENSP00000510528.1:p.Gln880Ter
ENST00000687971.1:c.2305C>T	ENSP00000510788.1:p.Gln769Ter
ENST00000693060.1:c.2518C>T	ENSP00000510329.1:p.Gln840Ter
ENST00000345136.8:c.2587C>T MANE Select	ENSP00000344848.3:p.Gln863Ter
ENST00000527303.2:c.2668C>T	ENSP00000433982.2:p.Gln890Ter
ENST00000322810.8:c.2998C>T	ENSP00000323856.4:p.Gln1000Ter
ENST00000345136.7:c.2587C>T	ENSP00000344848.3:p.Gln863Ter
ENST00000354589.7:c.2587C>T	ENSP00000346602.3:p.Gln863Ter
ENST00000354958.6:c.2521C>T	ENSP00000347044.2:p.Gln841Ter
ENST00000356346.7:c.2545C>T MANE Plus Clinical	ENSP00000348702.3:p.Gln849Ter
ENST00000357649.6:c.2599C>T	ENSP00000350277.2:p.Gln867Ter
ENST00000398774.6:c.2491C>T	ENSP00000381756.2:p.Gln831Ter
ENST00000436759.6:c.2668C>T	ENSP00000388180.2:p.Gln890Ter
ENST00000527096.5:c.2656C>T	ENSP00000434583.1:p.Gln886Ter
NM_000445.4:c.2668C>T	NP_000436.2:p.Gln890Ter
NM_201378.3:c.2545C>T	NP_958780.1:p.Gln849Ter
NM_201379.2:c.2521C>T	NP_958781.1:p.Gln841Ter
NM_201380.3:c.2998C>T	NP_958782.1:p.Gln1000Ter
NM_201381.2:c.2491C>T	NP_958783.1:p.Gln831Ter
NM_201382.3:c.2587C>T	NP_958784.1:p.Gln863Ter
NM_201383.2:c.2599C>T	NP_958785.1:p.Gln867Ter
NM_201384.2:c.2587C>T	NP_958786.1:p.Gln863Ter
XM_005250976.2:c.3013C>T	XP_005251033.1:p.Gln1005Ter
XM_005250978.2:c.2614C>T	XP_005251035.1:p.Gln872Ter
XM_005250979.3:c.2602C>T	XP_005251036.1:p.Gln868Ter
XM_005250980.3:c.2602C>T	XP_005251037.1:p.Gln868Ter
XM_005250981.2:c.2560C>T	XP_005251038.1:p.Gln854Ter
XM_005250982.2:c.2536C>T	XP_005251039.1:p.Gln846Ter
XM_005250983.2:c.2518C>T	XP_005251040.1:p.Gln840Ter
XM_005250984.3:c.2506C>T	XP_005251041.1:p.Gln836Ter
XM_006716588.2:c.2683C>T	XP_006716651.1:p.Gln895Ter
XM_006716589.2:c.2533C>T	XP_006716652.1:p.Gln845Ter
XM_006716590.2:c.2533C>T	XP_006716653.1:p.Gln845Ter
XM_011517130.1:c.2602C>T	XP_011515432.1:p.Gln868Ter
XM_011517131.1:c.2518C>T	XP_011515433.1:p.Gln840Ter
XM_011517132.1:c.2614C>T	XP_011515434.1:p.Gln872Ter
XM_005250976.4:c.3013C>T	XP_005251033.1:p.Gln1005Ter
XM_005250978.3:c.2614C>T	XP_005251035.1:p.Gln872Ter
XM_005250979.4:c.2602C>T	XP_005251036.1:p.Gln868Ter
XM_005250980.4:c.2602C>T	XP_005251037.1:p.Gln868Ter
XM_005250981.3:c.2560C>T	XP_005251038.1:p.Gln854Ter
XM_005250982.4:c.2536C>T	XP_005251039.1:p.Gln846Ter
XM_005250984.5:c.2506C>T	XP_005251041.1:p.Gln836Ter
XM_006716588.3:c.2683C>T	XP_006716651.1:p.Gln895Ter
XM_006716590.3:c.2533C>T	XP_006716653.1:p.Gln845Ter
XM_011517130.2:c.2602C>T	XP_011515432.1:p.Gln868Ter
XM_011517131.2:c.2518C>T	XP_011515433.1:p.Gln840Ter
XM_011517132.2:c.2614C>T	XP_011515434.1:p.Gln872Ter
NM_000445.5:c.2668C>T	NP_000436.2:p.Gln890Ter
NM_201378.4:c.2545C>T MANE Plus Clinical	NP_958780.1:p.Gln849Ter
NM_201379.3:c.2521C>T	NP_958781.1:p.Gln841Ter
NM_201380.4:c.2998C>T	NP_958782.1:p.Gln1000Ter
NM_201381.3:c.2491C>T	NP_958783.1:p.Gln831Ter
NM_201382.4:c.2587C>T	NP_958784.1:p.Gln863Ter
NM_201383.3:c.2599C>T	NP_958785.1:p.Gln867Ter
NM_201384.3:c.2587C>T MANE Select	NP_958786.1:p.Gln863Ter