Canonical Allele Identifier: CA2689011290
Gene: PLEC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.143916637_143916639del , CM000670.2:g.143916637_143916639del GRCh38
NC_000008.10:g.144990805_144990807del , CM000670.1:g.144990805_144990807del GRCh37
NC_000008.9:g.145062793_145062795del NCBI36
NG_012492.1:g.65111_65113del

Transcript Alleles

HGVS Amino-acid Change
ENST00000528025.6:c.13318_13320del ENSP00000437303.2:p.Gly4440del
ENST00000685198.1:c.13237_13239del ENSP00000510528.1:p.Gly4413del
ENST00000687971.1:c.12904_12906del ENSP00000510788.1:p.Gly4302del
ENST00000693060.1:c.13117_13119del ENSP00000510329.1:p.Gly4373del
ENST00000345136.8:c.13186_13188del MANE Select ENSP00000344848.3:p.Gly4396del
ENST00000527303.2:c.9886_9888del ENSP00000433982.2:p.Gly3296del
ENST00000322810.8:c.13597_13599del ENSP00000323856.4:p.Gly4533del
ENST00000345136.7:c.13186_13188del ENSP00000344848.3:p.Gly4396del
ENST00000354589.7:c.13186_13188del ENSP00000346602.3:p.Gly4396del
ENST00000354958.6:c.13120_13122del ENSP00000347044.2:p.Gly4374del
ENST00000356346.7:c.13144_13146del MANE Plus Clinical ENSP00000348702.3:p.Gly4382del
ENST00000357649.6:c.13198_13200del ENSP00000350277.2:p.Gly4400del
ENST00000398774.6:c.13090_13092del ENSP00000381756.2:p.Gly4364del
ENST00000436759.6:c.13267_13269del ENSP00000388180.2:p.Gly4423del
ENST00000527096.5:c.13255_13257del ENSP00000434583.1:p.Gly4419del
NM_000445.4:c.13267_13269del NP_000436.2:p.Gly4423del
NM_201378.3:c.13144_13146del NP_958780.1:p.Gly4382del
NM_201379.2:c.13120_13122del NP_958781.1:p.Gly4374del
NM_201380.3:c.13597_13599del NP_958782.1:p.Gly4533del
NM_201381.2:c.13090_13092del NP_958783.1:p.Gly4364del
NM_201382.3:c.13186_13188del NP_958784.1:p.Gly4396del
NM_201383.2:c.13198_13200del NP_958785.1:p.Gly4400del
NM_201384.2:c.13186_13188del NP_958786.1:p.Gly4396del
XM_005250976.2:c.13612_13614del XP_005251033.1:p.Gly4538del
XM_005250978.2:c.13213_13215del XP_005251035.1:p.Gly4405del
XM_005250979.3:c.13201_13203del XP_005251036.1:p.Gly4401del
XM_005250980.3:c.13201_13203del XP_005251037.1:p.Gly4401del
XM_005250981.2:c.13159_13161del XP_005251038.1:p.Gly4387del
XM_005250982.2:c.13135_13137del XP_005251039.1:p.Gly4379del
XM_005250983.2:c.13117_13119del XP_005251040.1:p.Gly4373del
XM_005250984.3:c.13105_13107del XP_005251041.1:p.Gly4369del
XM_006716588.2:c.13282_13284del XP_006716651.1:p.Gly4428del
XM_006716589.2:c.13132_13134del XP_006716652.1:p.Gly4378del
XM_006716590.2:c.13132_13134del XP_006716653.1:p.Gly4378del
XM_011517130.1:c.13201_13203del XP_011515432.1:p.Gly4401del
XM_011517131.1:c.13117_13119del XP_011515433.1:p.Gly4373del
XM_011517132.1:c.9832_9834del XP_011515434.1:p.Gly3278del
XM_005250976.4:c.13612_13614del XP_005251033.1:p.Gly4538del
XM_005250978.3:c.13213_13215del XP_005251035.1:p.Gly4405del
XM_005250979.4:c.13201_13203del XP_005251036.1:p.Gly4401del
XM_005250980.4:c.13201_13203del XP_005251037.1:p.Gly4401del
XM_005250981.3:c.13159_13161del XP_005251038.1:p.Gly4387del
XM_005250982.4:c.13135_13137del XP_005251039.1:p.Gly4379del
XM_005250984.5:c.13105_13107del XP_005251041.1:p.Gly4369del
XM_006716588.3:c.13282_13284del XP_006716651.1:p.Gly4428del
XM_006716590.3:c.13132_13134del XP_006716653.1:p.Gly4378del
XM_011517130.2:c.13201_13203del XP_011515432.1:p.Gly4401del
XM_011517131.2:c.13117_13119del XP_011515433.1:p.Gly4373del
XM_011517132.2:c.9832_9834del XP_011515434.1:p.Gly3278del
NM_000445.5:c.13267_13269del NP_000436.2:p.Gly4423del
NM_201378.4:c.13144_13146del MANE Plus Clinical NP_958780.1:p.Gly4382del
NM_201379.3:c.13120_13122del NP_958781.1:p.Gly4374del
NM_201380.4:c.13597_13599del NP_958782.1:p.Gly4533del
NM_201381.3:c.13090_13092del NP_958783.1:p.Gly4364del
NM_201382.4:c.13186_13188del NP_958784.1:p.Gly4396del
NM_201383.3:c.13198_13200del NP_958785.1:p.Gly4400del
NM_201384.3:c.13186_13188del MANE Select NP_958786.1:p.Gly4396del