Canonical Allele Identifier: CA1826037013

Gene: PLEC

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143916354_143916366delinsGGAGCCAGCGGTA , CM000670.2:g.143916354_143916366delinsGGAGCCAGCGGTA	GRCh38
NC_000008.10:g.144990522_144990534delinsGGAGCCAGCGGTA , CM000670.1:g.144990522_144990534delinsGGAGCCAGCGGTA	GRCh37
NC_000008.9:g.145062510_145062522delinsGGAGCCAGCGGTA	NCBI36
NG_012492.1:g.65380_65392delinsTACCGCTGGCTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528025.6:c.13587_13599delinsTACCGCTGGCTCC	ENSP00000437303.2:p.Ser4529=
ENST00000685198.1:c.13506_13518delinsTACCGCTGGCTCC	ENSP00000510528.1:p.Ser4502=
ENST00000687971.1:c.13173_13185delinsTACCGCTGGCTCC	ENSP00000510788.1:p.Ser4391=
ENST00000693060.1:c.13386_13398delinsTACCGCTGGCTCC	ENSP00000510329.1:p.Ser4462=
ENST00000345136.8:c.13455_13467delinsTACCGCTGGCTCC MANE Select	ENSP00000344848.3:p.Ser4485=
ENST00000527303.2:c.10155_10167delinsTACCGCTGGCTCC	ENSP00000433982.2:p.Ser3385=
ENST00000322810.8:c.13866_13878delinsTACCGCTGGCTCC	ENSP00000323856.4:p.Ser4622=
ENST00000345136.7:c.13455_13467delinsTACCGCTGGCTCC	ENSP00000344848.3:p.Ser4485=
ENST00000354589.7:c.13455_13467delinsTACCGCTGGCTCC	ENSP00000346602.3:p.Ser4485=
ENST00000354958.6:c.13389_13401delinsTACCGCTGGCTCC	ENSP00000347044.2:p.Ser4463=
ENST00000356346.7:c.13413_13425delinsTACCGCTGGCTCC MANE Plus Clinical	ENSP00000348702.3:p.Ser4471=
ENST00000357649.6:c.13467_13479delinsTACCGCTGGCTCC	ENSP00000350277.2:p.Ser4489=
ENST00000398774.6:c.13359_13371delinsTACCGCTGGCTCC	ENSP00000381756.2:p.Ser4453=
ENST00000436759.6:c.13536_13548delinsTACCGCTGGCTCC	ENSP00000388180.2:p.Ser4512=
ENST00000527096.5:c.13524_13536delinsTACCGCTGGCTCC	ENSP00000434583.1:p.Ser4508=
NM_000445.4:c.13536_13548delinsTACCGCTGGCTCC	NP_000436.2:p.Ser4512=
NM_201378.3:c.13413_13425delinsTACCGCTGGCTCC	NP_958780.1:p.Ser4471=
NM_201379.2:c.13389_13401delinsTACCGCTGGCTCC	NP_958781.1:p.Ser4463=
NM_201380.3:c.13866_13878delinsTACCGCTGGCTCC	NP_958782.1:p.Ser4622=
NM_201381.2:c.13359_13371delinsTACCGCTGGCTCC	NP_958783.1:p.Ser4453=
NM_201382.3:c.13455_13467delinsTACCGCTGGCTCC	NP_958784.1:p.Ser4485=
NM_201383.2:c.13467_13479delinsTACCGCTGGCTCC	NP_958785.1:p.Ser4489=
NM_201384.2:c.13455_13467delinsTACCGCTGGCTCC	NP_958786.1:p.Ser4485=
XM_005250976.2:c.13881_13893delinsTACCGCTGGCTCC	XP_005251033.1:p.Ser4627=
XM_005250978.2:c.13482_13494delinsTACCGCTGGCTCC	XP_005251035.1:p.Ser4494=
XM_005250979.3:c.13470_13482delinsTACCGCTGGCTCC	XP_005251036.1:p.Ser4490=
XM_005250980.3:c.13470_13482delinsTACCGCTGGCTCC	XP_005251037.1:p.Ser4490=
XM_005250981.2:c.13428_13440delinsTACCGCTGGCTCC	XP_005251038.1:p.Ser4476=
XM_005250982.2:c.13404_13416delinsTACCGCTGGCTCC	XP_005251039.1:p.Ser4468=
XM_005250983.2:c.13386_13398delinsTACCGCTGGCTCC	XP_005251040.1:p.Ser4462=
XM_005250984.3:c.13374_13386delinsTACCGCTGGCTCC	XP_005251041.1:p.Ser4458=
XM_006716588.2:c.13551_13563delinsTACCGCTGGCTCC	XP_006716651.1:p.Ser4517=
XM_006716589.2:c.13401_13413delinsTACCGCTGGCTCC	XP_006716652.1:p.Ser4467=
XM_006716590.2:c.13401_13413delinsTACCGCTGGCTCC	XP_006716653.1:p.Ser4467=
XM_011517130.1:c.13470_13482delinsTACCGCTGGCTCC	XP_011515432.1:p.Ser4490=
XM_011517131.1:c.13386_13398delinsTACCGCTGGCTCC	XP_011515433.1:p.Ser4462=
XM_011517132.1:c.10101_10113delinsTACCGCTGGCTCC	XP_011515434.1:p.Ser3367=
XM_005250976.4:c.13881_13893delinsTACCGCTGGCTCC	XP_005251033.1:p.Ser4627=
XM_005250978.3:c.13482_13494delinsTACCGCTGGCTCC	XP_005251035.1:p.Ser4494=
XM_005250979.4:c.13470_13482delinsTACCGCTGGCTCC	XP_005251036.1:p.Ser4490=
XM_005250980.4:c.13470_13482delinsTACCGCTGGCTCC	XP_005251037.1:p.Ser4490=
XM_005250981.3:c.13428_13440delinsTACCGCTGGCTCC	XP_005251038.1:p.Ser4476=
XM_005250982.4:c.13404_13416delinsTACCGCTGGCTCC	XP_005251039.1:p.Ser4468=
XM_005250984.5:c.13374_13386delinsTACCGCTGGCTCC	XP_005251041.1:p.Ser4458=
XM_006716588.3:c.13551_13563delinsTACCGCTGGCTCC	XP_006716651.1:p.Ser4517=
XM_006716590.3:c.13401_13413delinsTACCGCTGGCTCC	XP_006716653.1:p.Ser4467=
XM_011517130.2:c.13470_13482delinsTACCGCTGGCTCC	XP_011515432.1:p.Ser4490=
XM_011517131.2:c.13386_13398delinsTACCGCTGGCTCC	XP_011515433.1:p.Ser4462=
XM_011517132.2:c.10101_10113delinsTACCGCTGGCTCC	XP_011515434.1:p.Ser3367=
NM_000445.5:c.13536_13548delinsTACCGCTGGCTCC	NP_000436.2:p.Ser4512=
NM_201378.4:c.13413_13425delinsTACCGCTGGCTCC MANE Plus Clinical	NP_958780.1:p.Ser4471=
NM_201379.3:c.13389_13401delinsTACCGCTGGCTCC	NP_958781.1:p.Ser4463=
NM_201380.4:c.13866_13878delinsTACCGCTGGCTCC	NP_958782.1:p.Ser4622=
NM_201381.3:c.13359_13371delinsTACCGCTGGCTCC	NP_958783.1:p.Ser4453=
NM_201382.4:c.13455_13467delinsTACCGCTGGCTCC	NP_958784.1:p.Ser4485=
NM_201383.3:c.13467_13479delinsTACCGCTGGCTCC	NP_958785.1:p.Ser4489=
NM_201384.3:c.13455_13467delinsTACCGCTGGCTCC MANE Select	NP_958786.1:p.Ser4485=