Canonical Allele Identifier: CA4928422
Community Standard Title: NM_201384.3(PLEC):c.477G>A (p.Thr159=)
Gene: PLEC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.143935973C>T , CM000670.2:g.143935973C>T GRCh38
NC_000008.10:g.145010141C>T , CM000670.1:g.145010141C>T GRCh37
NC_000008.9:g.145082129C>T NCBI36
NG_012492.1:g.45773G>A

Transcript Alleles

HGVS Amino-acid Change
NM_201384.3:c.477G>A MANE Select NP_958786.1:p.Thr159=
ENST00000345136.8:c.477G>A MANE Select ENSP00000344848.3:p.Thr159=
NM_201378.4:c.435G>A MANE Plus Clinical NP_958780.1:p.Thr145=
ENST00000356346.7:c.435G>A MANE Plus Clinical ENSP00000348702.3:p.Thr145=
NM_000445.4:c.558G>A NP_000436.2:p.Thr186=
NM_000445.5:c.558G>A NP_000436.2:p.Thr186=
NM_201378.3:c.435G>A NP_958780.1:p.Thr145=
NM_201379.2:c.411G>A NP_958781.1:p.Thr137=
NM_201379.3:c.411G>A NP_958781.1:p.Thr137=
NM_201380.3:c.888G>A NP_958782.1:p.Thr296=
NM_201380.4:c.888G>A NP_958782.1:p.Thr296=
NM_201381.2:c.381G>A NP_958783.1:p.Thr127=
NM_201381.3:c.381G>A NP_958783.1:p.Thr127=
NM_201382.3:c.477G>A NP_958784.1:p.Thr159=
NM_201382.4:c.477G>A NP_958784.1:p.Thr159=
NM_201383.2:c.489G>A NP_958785.1:p.Thr163=
NM_201383.3:c.489G>A NP_958785.1:p.Thr163=
NM_201384.2:c.477G>A NP_958786.1:p.Thr159=
ENST00000322810.8:c.888G>A ENSP00000323856.4:p.Thr296=
ENST00000345136.7:c.477G>A ENSP00000344848.3:p.Thr159=
ENST00000354589.7:c.477G>A ENSP00000346602.3:p.Thr159=
ENST00000354958.6:c.411G>A ENSP00000347044.2:p.Thr137=
ENST00000357649.6:c.489G>A ENSP00000350277.2:p.Thr163=
ENST00000398774.6:c.381G>A ENSP00000381756.2:p.Thr127=
ENST00000436759.6:c.558G>A ENSP00000388180.2:p.Thr186=
ENST00000526416.5:c.408G>A ENSP00000433557.1:p.Thr136=
ENST00000527096.5:c.558G>A ENSP00000434583.1:p.Thr186=
ENST00000527303.2:c.558G>A ENSP00000433982.2:p.Thr186=
ENST00000527816.5:c.195G>A ENSP00000434490.1:p.Thr65=
ENST00000528025.5:c.609G>A ENSP00000437303.1:p.Thr203=
ENST00000528025.6:c.609G>A ENSP00000437303.2:p.Thr203=
ENST00000685198.1:c.528G>A ENSP00000510528.1:p.Thr176=
ENST00000687971.1:c.195G>A ENSP00000510788.1:p.Thr65=
ENST00000693060.1:c.408G>A ENSP00000510329.1:p.Thr136=
XM_005250976.2:c.903G>A XP_005251033.1:p.Thr301=
XM_005250976.4:c.903G>A XP_005251033.1:p.Thr301=
XM_005250978.2:c.504G>A XP_005251035.1:p.Thr168=
XM_005250978.3:c.504G>A XP_005251035.1:p.Thr168=
XM_005250979.3:c.492G>A XP_005251036.1:p.Thr164=
XM_005250979.4:c.492G>A XP_005251036.1:p.Thr164=
XM_005250980.3:c.492G>A XP_005251037.1:p.Thr164=
XM_005250980.4:c.492G>A XP_005251037.1:p.Thr164=
XM_005250981.2:c.450G>A XP_005251038.1:p.Thr150=
XM_005250981.3:c.450G>A XP_005251038.1:p.Thr150=
XM_005250982.2:c.426G>A XP_005251039.1:p.Thr142=
XM_005250982.4:c.426G>A XP_005251039.1:p.Thr142=
XM_005250983.2:c.408G>A XP_005251040.1:p.Thr136=
XM_005250984.3:c.396G>A XP_005251041.1:p.Thr132=
XM_005250984.5:c.396G>A XP_005251041.1:p.Thr132=
XM_006716588.2:c.573G>A XP_006716651.1:p.Thr191=
XM_006716588.3:c.573G>A XP_006716651.1:p.Thr191=
XM_006716589.2:c.423G>A XP_006716652.1:p.Thr141=
XM_006716590.2:c.423G>A XP_006716653.1:p.Thr141=
XM_006716590.3:c.423G>A XP_006716653.1:p.Thr141=
XM_011517130.1:c.504G>A XP_011515432.1:p.Thr168=
XM_011517130.2:c.504G>A XP_011515432.1:p.Thr168=
XM_011517131.1:c.408G>A XP_011515433.1:p.Thr136=
XM_011517131.2:c.408G>A XP_011515433.1:p.Thr136=
XM_011517132.1:c.504G>A XP_011515434.1:p.Thr168=
XM_011517132.2:c.504G>A XP_011515434.1:p.Thr168=