Canonical Allele Identifier: CA372476134

Gene: PLEC

Linked Data

• gnomAD v4: 8-143916641-T-A
• MyVariant Identifiers: chr8:g.144990809T>A (hg19) ; chr8:g.143916641T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143916641T>A , CM000670.2:g.143916641T>A	GRCh38
NC_000008.10:g.144990809T>A , CM000670.1:g.144990809T>A	GRCh37
NC_000008.9:g.145062797T>A	NCBI36
NG_012492.1:g.65105A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528025.6:c.13312A>T	ENSP00000437303.2:p.Thr4438Ser
ENST00000685198.1:c.13231A>T	ENSP00000510528.1:p.Thr4411Ser
ENST00000687971.1:c.12898A>T	ENSP00000510788.1:p.Thr4300Ser
ENST00000693060.1:c.13111A>T	ENSP00000510329.1:p.Thr4371Ser
ENST00000345136.8:c.13180A>T MANE Select	ENSP00000344848.3:p.Thr4394Ser
ENST00000527303.2:c.9880A>T	ENSP00000433982.2:p.Thr3294Ser
ENST00000322810.8:c.13591A>T	ENSP00000323856.4:p.Thr4531Ser
ENST00000345136.7:c.13180A>T	ENSP00000344848.3:p.Thr4394Ser
ENST00000354589.7:c.13180A>T	ENSP00000346602.3:p.Thr4394Ser
ENST00000354958.6:c.13114A>T	ENSP00000347044.2:p.Thr4372Ser
ENST00000356346.7:c.13138A>T MANE Plus Clinical	ENSP00000348702.3:p.Thr4380Ser
ENST00000357649.6:c.13192A>T	ENSP00000350277.2:p.Thr4398Ser
ENST00000398774.6:c.13084A>T	ENSP00000381756.2:p.Thr4362Ser
ENST00000436759.6:c.13261A>T	ENSP00000388180.2:p.Thr4421Ser
ENST00000527096.5:c.13249A>T	ENSP00000434583.1:p.Thr4417Ser
NM_000445.4:c.13261A>T	NP_000436.2:p.Thr4421Ser
NM_201378.3:c.13138A>T	NP_958780.1:p.Thr4380Ser
NM_201379.2:c.13114A>T	NP_958781.1:p.Thr4372Ser
NM_201380.3:c.13591A>T	NP_958782.1:p.Thr4531Ser
NM_201381.2:c.13084A>T	NP_958783.1:p.Thr4362Ser
NM_201382.3:c.13180A>T	NP_958784.1:p.Thr4394Ser
NM_201383.2:c.13192A>T	NP_958785.1:p.Thr4398Ser
NM_201384.2:c.13180A>T	NP_958786.1:p.Thr4394Ser
XM_005250976.2:c.13606A>T	XP_005251033.1:p.Thr4536Ser
XM_005250978.2:c.13207A>T	XP_005251035.1:p.Thr4403Ser
XM_005250979.3:c.13195A>T	XP_005251036.1:p.Thr4399Ser
XM_005250980.3:c.13195A>T	XP_005251037.1:p.Thr4399Ser
XM_005250981.2:c.13153A>T	XP_005251038.1:p.Thr4385Ser
XM_005250982.2:c.13129A>T	XP_005251039.1:p.Thr4377Ser
XM_005250983.2:c.13111A>T	XP_005251040.1:p.Thr4371Ser
XM_005250984.3:c.13099A>T	XP_005251041.1:p.Thr4367Ser
XM_006716588.2:c.13276A>T	XP_006716651.1:p.Thr4426Ser
XM_006716589.2:c.13126A>T	XP_006716652.1:p.Thr4376Ser
XM_006716590.2:c.13126A>T	XP_006716653.1:p.Thr4376Ser
XM_011517130.1:c.13195A>T	XP_011515432.1:p.Thr4399Ser
XM_011517131.1:c.13111A>T	XP_011515433.1:p.Thr4371Ser
XM_011517132.1:c.9826A>T	XP_011515434.1:p.Thr3276Ser
XM_005250976.4:c.13606A>T	XP_005251033.1:p.Thr4536Ser
XM_005250978.3:c.13207A>T	XP_005251035.1:p.Thr4403Ser
XM_005250979.4:c.13195A>T	XP_005251036.1:p.Thr4399Ser
XM_005250980.4:c.13195A>T	XP_005251037.1:p.Thr4399Ser
XM_005250981.3:c.13153A>T	XP_005251038.1:p.Thr4385Ser
XM_005250982.4:c.13129A>T	XP_005251039.1:p.Thr4377Ser
XM_005250984.5:c.13099A>T	XP_005251041.1:p.Thr4367Ser
XM_006716588.3:c.13276A>T	XP_006716651.1:p.Thr4426Ser
XM_006716590.3:c.13126A>T	XP_006716653.1:p.Thr4376Ser
XM_011517130.2:c.13195A>T	XP_011515432.1:p.Thr4399Ser
XM_011517131.2:c.13111A>T	XP_011515433.1:p.Thr4371Ser
XM_011517132.2:c.9826A>T	XP_011515434.1:p.Thr3276Ser
NM_000445.5:c.13261A>T	NP_000436.2:p.Thr4421Ser
NM_201378.4:c.13138A>T MANE Plus Clinical	NP_958780.1:p.Thr4380Ser
NM_201379.3:c.13114A>T	NP_958781.1:p.Thr4372Ser
NM_201380.4:c.13591A>T	NP_958782.1:p.Thr4531Ser
NM_201381.3:c.13084A>T	NP_958783.1:p.Thr4362Ser
NM_201382.4:c.13180A>T	NP_958784.1:p.Thr4394Ser
NM_201383.3:c.13192A>T	NP_958785.1:p.Thr4398Ser
NM_201384.3:c.13180A>T MANE Select	NP_958786.1:p.Thr4394Ser