Canonical Allele Identifier: CA463526141

Gene: PLEC

Linked Data

• MyVariant Identifiers: chr8:g.144990498G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143916330G>C , CM000670.2:g.143916330G>C	GRCh38
NC_000008.10:g.144990498G>C , CM000670.1:g.144990498G>C	GRCh37
NC_000008.9:g.145062486G>C	NCBI36
NG_012492.1:g.65416C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528025.6:c.13623C>G	ENSP00000437303.2:p.Ser4541=
ENST00000685198.1:c.13542C>G	ENSP00000510528.1:p.Ser4514=
ENST00000687971.1:c.13209C>G	ENSP00000510788.1:p.Ser4403=
ENST00000693060.1:c.13422C>G	ENSP00000510329.1:p.Ser4474=
ENST00000345136.8:c.13491C>G MANE Select	ENSP00000344848.3:p.Ser4497=
ENST00000527303.2:c.10191C>G	ENSP00000433982.2:p.Ser3397=
ENST00000322810.8:c.13902C>G	ENSP00000323856.4:p.Ser4634=
ENST00000345136.7:c.13491C>G	ENSP00000344848.3:p.Ser4497=
ENST00000354589.7:c.13491C>G	ENSP00000346602.3:p.Ser4497=
ENST00000354958.6:c.13425C>G	ENSP00000347044.2:p.Ser4475=
ENST00000356346.7:c.13449C>G MANE Plus Clinical	ENSP00000348702.3:p.Ser4483=
ENST00000357649.6:c.13503C>G	ENSP00000350277.2:p.Ser4501=
ENST00000398774.6:c.13395C>G	ENSP00000381756.2:p.Ser4465=
ENST00000436759.6:c.13572C>G	ENSP00000388180.2:p.Ser4524=
ENST00000527096.5:c.13560C>G	ENSP00000434583.1:p.Ser4520=
NM_000445.4:c.13572C>G	NP_000436.2:p.Ser4524=
NM_201378.3:c.13449C>G	NP_958780.1:p.Ser4483=
NM_201379.2:c.13425C>G	NP_958781.1:p.Ser4475=
NM_201380.3:c.13902C>G	NP_958782.1:p.Ser4634=
NM_201381.2:c.13395C>G	NP_958783.1:p.Ser4465=
NM_201382.3:c.13491C>G	NP_958784.1:p.Ser4497=
NM_201383.2:c.13503C>G	NP_958785.1:p.Ser4501=
NM_201384.2:c.13491C>G	NP_958786.1:p.Ser4497=
XM_005250976.2:c.13917C>G	XP_005251033.1:p.Ser4639=
XM_005250978.2:c.13518C>G	XP_005251035.1:p.Ser4506=
XM_005250979.3:c.13506C>G	XP_005251036.1:p.Ser4502=
XM_005250980.3:c.13506C>G	XP_005251037.1:p.Ser4502=
XM_005250981.2:c.13464C>G	XP_005251038.1:p.Ser4488=
XM_005250982.2:c.13440C>G	XP_005251039.1:p.Ser4480=
XM_005250983.2:c.13422C>G	XP_005251040.1:p.Ser4474=
XM_005250984.3:c.13410C>G	XP_005251041.1:p.Ser4470=
XM_006716588.2:c.13587C>G	XP_006716651.1:p.Ser4529=
XM_006716589.2:c.13437C>G	XP_006716652.1:p.Ser4479=
XM_006716590.2:c.13437C>G	XP_006716653.1:p.Ser4479=
XM_011517130.1:c.13506C>G	XP_011515432.1:p.Ser4502=
XM_011517131.1:c.13422C>G	XP_011515433.1:p.Ser4474=
XM_011517132.1:c.10137C>G	XP_011515434.1:p.Ser3379=
XM_005250976.4:c.13917C>G	XP_005251033.1:p.Ser4639=
XM_005250978.3:c.13518C>G	XP_005251035.1:p.Ser4506=
XM_005250979.4:c.13506C>G	XP_005251036.1:p.Ser4502=
XM_005250980.4:c.13506C>G	XP_005251037.1:p.Ser4502=
XM_005250981.3:c.13464C>G	XP_005251038.1:p.Ser4488=
XM_005250982.4:c.13440C>G	XP_005251039.1:p.Ser4480=
XM_005250984.5:c.13410C>G	XP_005251041.1:p.Ser4470=
XM_006716588.3:c.13587C>G	XP_006716651.1:p.Ser4529=
XM_006716590.3:c.13437C>G	XP_006716653.1:p.Ser4479=
XM_011517130.2:c.13506C>G	XP_011515432.1:p.Ser4502=
XM_011517131.2:c.13422C>G	XP_011515433.1:p.Ser4474=
XM_011517132.2:c.10137C>G	XP_011515434.1:p.Ser3379=
NM_000445.5:c.13572C>G	NP_000436.2:p.Ser4524=
NM_201378.4:c.13449C>G MANE Plus Clinical	NP_958780.1:p.Ser4483=
NM_201379.3:c.13425C>G	NP_958781.1:p.Ser4475=
NM_201380.4:c.13902C>G	NP_958782.1:p.Ser4634=
NM_201381.3:c.13395C>G	NP_958783.1:p.Ser4465=
NM_201382.4:c.13491C>G	NP_958784.1:p.Ser4497=
NM_201383.3:c.13503C>G	NP_958785.1:p.Ser4501=
NM_201384.3:c.13491C>G MANE Select	NP_958786.1:p.Ser4497=