Canonical Allele Identifier: CA4924927

Gene: PLEC

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143920245G>A , CM000670.2:g.143920245G>A	GRCh38
NC_000008.10:g.144994413G>A , CM000670.1:g.144994413G>A	GRCh37
NC_000008.9:g.145066401G>A	NCBI36
NG_012492.1:g.61501C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_201384.3:c.9576C>T MANE Select	NP_958786.1:p.Tyr3192=
ENST00000345136.8:c.9576C>T MANE Select	ENSP00000344848.3:p.Tyr3192=
NM_201378.4:c.9534C>T MANE Plus Clinical	NP_958780.1:p.Tyr3178=
ENST00000356346.7:c.9534C>T MANE Plus Clinical	ENSP00000348702.3:p.Tyr3178=
NM_000445.4:c.9657C>T	NP_000436.2:p.Tyr3219=
NM_000445.5:c.9657C>T	NP_000436.2:p.Tyr3219=
NM_201378.3:c.9534C>T	NP_958780.1:p.Tyr3178=
NM_201379.2:c.9510C>T	NP_958781.1:p.Tyr3170=
NM_201379.3:c.9510C>T	NP_958781.1:p.Tyr3170=
NM_201380.3:c.9987C>T	NP_958782.1:p.Tyr3329=
NM_201380.4:c.9987C>T	NP_958782.1:p.Tyr3329=
NM_201381.2:c.9480C>T	NP_958783.1:p.Tyr3160=
NM_201381.3:c.9480C>T	NP_958783.1:p.Tyr3160=
NM_201382.3:c.9576C>T	NP_958784.1:p.Tyr3192=
NM_201382.4:c.9576C>T	NP_958784.1:p.Tyr3192=
NM_201383.2:c.9588C>T	NP_958785.1:p.Tyr3196=
NM_201383.3:c.9588C>T	NP_958785.1:p.Tyr3196=
NM_201384.2:c.9576C>T	NP_958786.1:p.Tyr3192=
ENST00000322810.8:c.9987C>T	ENSP00000323856.4:p.Tyr3329=
ENST00000345136.7:c.9576C>T	ENSP00000344848.3:p.Tyr3192=
ENST00000354589.7:c.9576C>T	ENSP00000346602.3:p.Tyr3192=
ENST00000354958.6:c.9510C>T	ENSP00000347044.2:p.Tyr3170=
ENST00000357649.6:c.9588C>T	ENSP00000350277.2:p.Tyr3196=
ENST00000398774.6:c.9480C>T	ENSP00000381756.2:p.Tyr3160=
ENST00000436759.6:c.9657C>T	ENSP00000388180.2:p.Tyr3219=
ENST00000527096.5:c.9645C>T	ENSP00000434583.1:p.Tyr3215=
ENST00000527303.2:c.6276C>T	ENSP00000433982.2:p.Tyr2092=
ENST00000528025.6:c.9708C>T	ENSP00000437303.2:p.Tyr3236=
ENST00000685198.1:c.9627C>T	ENSP00000510528.1:p.Tyr3209=
ENST00000687971.1:c.9294C>T	ENSP00000510788.1:p.Tyr3098=
ENST00000693060.1:c.9507C>T	ENSP00000510329.1:p.Tyr3169=
XM_005250976.2:c.10002C>T	XP_005251033.1:p.Tyr3334=
XM_005250976.4:c.10002C>T	XP_005251033.1:p.Tyr3334=
XM_005250978.2:c.9603C>T	XP_005251035.1:p.Tyr3201=
XM_005250978.3:c.9603C>T	XP_005251035.1:p.Tyr3201=
XM_005250979.3:c.9591C>T	XP_005251036.1:p.Tyr3197=
XM_005250979.4:c.9591C>T	XP_005251036.1:p.Tyr3197=
XM_005250980.3:c.9591C>T	XP_005251037.1:p.Tyr3197=
XM_005250980.4:c.9591C>T	XP_005251037.1:p.Tyr3197=
XM_005250981.2:c.9549C>T	XP_005251038.1:p.Tyr3183=
XM_005250981.3:c.9549C>T	XP_005251038.1:p.Tyr3183=
XM_005250982.2:c.9525C>T	XP_005251039.1:p.Tyr3175=
XM_005250982.4:c.9525C>T	XP_005251039.1:p.Tyr3175=
XM_005250983.2:c.9507C>T	XP_005251040.1:p.Tyr3169=
XM_005250984.3:c.9495C>T	XP_005251041.1:p.Tyr3165=
XM_005250984.5:c.9495C>T	XP_005251041.1:p.Tyr3165=
XM_006716588.2:c.9672C>T	XP_006716651.1:p.Tyr3224=
XM_006716588.3:c.9672C>T	XP_006716651.1:p.Tyr3224=
XM_006716589.2:c.9522C>T	XP_006716652.1:p.Tyr3174=
XM_006716590.2:c.9522C>T	XP_006716653.1:p.Tyr3174=
XM_006716590.3:c.9522C>T	XP_006716653.1:p.Tyr3174=
XM_011517130.1:c.9591C>T	XP_011515432.1:p.Tyr3197=
XM_011517130.2:c.9591C>T	XP_011515432.1:p.Tyr3197=
XM_011517131.1:c.9507C>T	XP_011515433.1:p.Tyr3169=
XM_011517131.2:c.9507C>T	XP_011515433.1:p.Tyr3169=
XM_011517132.1:c.6222C>T	XP_011515434.1:p.Tyr2074=
XM_011517132.2:c.6222C>T	XP_011515434.1:p.Tyr2074=