Canonical Allele Identifier: CA372475721

Gene: PLEC

Linked Data

• MyVariant Identifiers: chr8:g.144990701C>A (hg19) ; chr8:g.143916533C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143916533C>A , CM000670.2:g.143916533C>A	GRCh38
NC_000008.10:g.144990701C>A , CM000670.1:g.144990701C>A	GRCh37
NC_000008.9:g.145062689C>A	NCBI36
NG_012492.1:g.65213G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528025.6:c.13420G>T	ENSP00000437303.2:p.Ala4474Ser
ENST00000685198.1:c.13339G>T	ENSP00000510528.1:p.Ala4447Ser
ENST00000687971.1:c.13006G>T	ENSP00000510788.1:p.Ala4336Ser
ENST00000693060.1:c.13219G>T	ENSP00000510329.1:p.Ala4407Ser
ENST00000345136.8:c.13288G>T MANE Select	ENSP00000344848.3:p.Ala4430Ser
ENST00000527303.2:c.9988G>T	ENSP00000433982.2:p.Ala3330Ser
ENST00000322810.8:c.13699G>T	ENSP00000323856.4:p.Ala4567Ser
ENST00000345136.7:c.13288G>T	ENSP00000344848.3:p.Ala4430Ser
ENST00000354589.7:c.13288G>T	ENSP00000346602.3:p.Ala4430Ser
ENST00000354958.6:c.13222G>T	ENSP00000347044.2:p.Ala4408Ser
ENST00000356346.7:c.13246G>T MANE Plus Clinical	ENSP00000348702.3:p.Ala4416Ser
ENST00000357649.6:c.13300G>T	ENSP00000350277.2:p.Ala4434Ser
ENST00000398774.6:c.13192G>T	ENSP00000381756.2:p.Ala4398Ser
ENST00000436759.6:c.13369G>T	ENSP00000388180.2:p.Ala4457Ser
ENST00000527096.5:c.13357G>T	ENSP00000434583.1:p.Ala4453Ser
NM_000445.4:c.13369G>T	NP_000436.2:p.Ala4457Ser
NM_201378.3:c.13246G>T	NP_958780.1:p.Ala4416Ser
NM_201379.2:c.13222G>T	NP_958781.1:p.Ala4408Ser
NM_201380.3:c.13699G>T	NP_958782.1:p.Ala4567Ser
NM_201381.2:c.13192G>T	NP_958783.1:p.Ala4398Ser
NM_201382.3:c.13288G>T	NP_958784.1:p.Ala4430Ser
NM_201383.2:c.13300G>T	NP_958785.1:p.Ala4434Ser
NM_201384.2:c.13288G>T	NP_958786.1:p.Ala4430Ser
XM_005250976.2:c.13714G>T	XP_005251033.1:p.Ala4572Ser
XM_005250978.2:c.13315G>T	XP_005251035.1:p.Ala4439Ser
XM_005250979.3:c.13303G>T	XP_005251036.1:p.Ala4435Ser
XM_005250980.3:c.13303G>T	XP_005251037.1:p.Ala4435Ser
XM_005250981.2:c.13261G>T	XP_005251038.1:p.Ala4421Ser
XM_005250982.2:c.13237G>T	XP_005251039.1:p.Ala4413Ser
XM_005250983.2:c.13219G>T	XP_005251040.1:p.Ala4407Ser
XM_005250984.3:c.13207G>T	XP_005251041.1:p.Ala4403Ser
XM_006716588.2:c.13384G>T	XP_006716651.1:p.Ala4462Ser
XM_006716589.2:c.13234G>T	XP_006716652.1:p.Ala4412Ser
XM_006716590.2:c.13234G>T	XP_006716653.1:p.Ala4412Ser
XM_011517130.1:c.13303G>T	XP_011515432.1:p.Ala4435Ser
XM_011517131.1:c.13219G>T	XP_011515433.1:p.Ala4407Ser
XM_011517132.1:c.9934G>T	XP_011515434.1:p.Ala3312Ser
XM_005250976.4:c.13714G>T	XP_005251033.1:p.Ala4572Ser
XM_005250978.3:c.13315G>T	XP_005251035.1:p.Ala4439Ser
XM_005250979.4:c.13303G>T	XP_005251036.1:p.Ala4435Ser
XM_005250980.4:c.13303G>T	XP_005251037.1:p.Ala4435Ser
XM_005250981.3:c.13261G>T	XP_005251038.1:p.Ala4421Ser
XM_005250982.4:c.13237G>T	XP_005251039.1:p.Ala4413Ser
XM_005250984.5:c.13207G>T	XP_005251041.1:p.Ala4403Ser
XM_006716588.3:c.13384G>T	XP_006716651.1:p.Ala4462Ser
XM_006716590.3:c.13234G>T	XP_006716653.1:p.Ala4412Ser
XM_011517130.2:c.13303G>T	XP_011515432.1:p.Ala4435Ser
XM_011517131.2:c.13219G>T	XP_011515433.1:p.Ala4407Ser
XM_011517132.2:c.9934G>T	XP_011515434.1:p.Ala3312Ser
NM_000445.5:c.13369G>T	NP_000436.2:p.Ala4457Ser
NM_201378.4:c.13246G>T MANE Plus Clinical	NP_958780.1:p.Ala4416Ser
NM_201379.3:c.13222G>T	NP_958781.1:p.Ala4408Ser
NM_201380.4:c.13699G>T	NP_958782.1:p.Ala4567Ser
NM_201381.3:c.13192G>T	NP_958783.1:p.Ala4398Ser
NM_201382.4:c.13288G>T	NP_958784.1:p.Ala4430Ser
NM_201383.3:c.13300G>T	NP_958785.1:p.Ala4434Ser
NM_201384.3:c.13288G>T MANE Select	NP_958786.1:p.Ala4430Ser