Canonical Allele Identifier: CA1826037254
Gene: PLEC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.143916480C= , CM000670.2:g.143916480C= GRCh38
NC_000008.10:g.144990648C= , CM000670.1:g.144990648C= GRCh37
NC_000008.9:g.145062636C= NCBI36
NG_012492.1:g.65266G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000528025.6:c.13473G= ENSP00000437303.2:p.Lys4491=
ENST00000685198.1:c.13392G= ENSP00000510528.1:p.Lys4464=
ENST00000687971.1:c.13059G= ENSP00000510788.1:p.Lys4353=
ENST00000693060.1:c.13272G= ENSP00000510329.1:p.Lys4424=
ENST00000345136.8:c.13341G= MANE Select ENSP00000344848.3:p.Lys4447=
ENST00000527303.2:c.10041G= ENSP00000433982.2:p.Lys3347=
ENST00000322810.8:c.13752G= ENSP00000323856.4:p.Lys4584=
ENST00000345136.7:c.13341G= ENSP00000344848.3:p.Lys4447=
ENST00000354589.7:c.13341G= ENSP00000346602.3:p.Lys4447=
ENST00000354958.6:c.13275G= ENSP00000347044.2:p.Lys4425=
ENST00000356346.7:c.13299G= MANE Plus Clinical ENSP00000348702.3:p.Lys4433=
ENST00000357649.6:c.13353G= ENSP00000350277.2:p.Lys4451=
ENST00000398774.6:c.13245G= ENSP00000381756.2:p.Lys4415=
ENST00000436759.6:c.13422G= ENSP00000388180.2:p.Lys4474=
ENST00000527096.5:c.13410G= ENSP00000434583.1:p.Lys4470=
NM_000445.4:c.13422G= NP_000436.2:p.Lys4474=
NM_201378.3:c.13299G= NP_958780.1:p.Lys4433=
NM_201379.2:c.13275G= NP_958781.1:p.Lys4425=
NM_201380.3:c.13752G= NP_958782.1:p.Lys4584=
NM_201381.2:c.13245G= NP_958783.1:p.Lys4415=
NM_201382.3:c.13341G= NP_958784.1:p.Lys4447=
NM_201383.2:c.13353G= NP_958785.1:p.Lys4451=
NM_201384.2:c.13341G= NP_958786.1:p.Lys4447=
XM_005250976.2:c.13767G= XP_005251033.1:p.Lys4589=
XM_005250978.2:c.13368G= XP_005251035.1:p.Lys4456=
XM_005250979.3:c.13356G= XP_005251036.1:p.Lys4452=
XM_005250980.3:c.13356G= XP_005251037.1:p.Lys4452=
XM_005250981.2:c.13314G= XP_005251038.1:p.Lys4438=
XM_005250982.2:c.13290G= XP_005251039.1:p.Lys4430=
XM_005250983.2:c.13272G= XP_005251040.1:p.Lys4424=
XM_005250984.3:c.13260G= XP_005251041.1:p.Lys4420=
XM_006716588.2:c.13437G= XP_006716651.1:p.Lys4479=
XM_006716589.2:c.13287G= XP_006716652.1:p.Lys4429=
XM_006716590.2:c.13287G= XP_006716653.1:p.Lys4429=
XM_011517130.1:c.13356G= XP_011515432.1:p.Lys4452=
XM_011517131.1:c.13272G= XP_011515433.1:p.Lys4424=
XM_011517132.1:c.9987G= XP_011515434.1:p.Lys3329=
XM_005250976.4:c.13767G= XP_005251033.1:p.Lys4589=
XM_005250978.3:c.13368G= XP_005251035.1:p.Lys4456=
XM_005250979.4:c.13356G= XP_005251036.1:p.Lys4452=
XM_005250980.4:c.13356G= XP_005251037.1:p.Lys4452=
XM_005250981.3:c.13314G= XP_005251038.1:p.Lys4438=
XM_005250982.4:c.13290G= XP_005251039.1:p.Lys4430=
XM_005250984.5:c.13260G= XP_005251041.1:p.Lys4420=
XM_006716588.3:c.13437G= XP_006716651.1:p.Lys4479=
XM_006716590.3:c.13287G= XP_006716653.1:p.Lys4429=
XM_011517130.2:c.13356G= XP_011515432.1:p.Lys4452=
XM_011517131.2:c.13272G= XP_011515433.1:p.Lys4424=
XM_011517132.2:c.9987G= XP_011515434.1:p.Lys3329=
NM_000445.5:c.13422G= NP_000436.2:p.Lys4474=
NM_201378.4:c.13299G= MANE Plus Clinical NP_958780.1:p.Lys4433=
NM_201379.3:c.13275G= NP_958781.1:p.Lys4425=
NM_201380.4:c.13752G= NP_958782.1:p.Lys4584=
NM_201381.3:c.13245G= NP_958783.1:p.Lys4415=
NM_201382.4:c.13341G= NP_958784.1:p.Lys4447=
NM_201383.3:c.13353G= NP_958785.1:p.Lys4451=
NM_201384.3:c.13341G= MANE Select NP_958786.1:p.Lys4447=