Canonical Allele Identifier: CA1769083548
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939466T= , CM000670.2:g.19939466T= GRCh38
NC_000008.10:g.19796977T= , CM000670.1:g.19796977T= GRCh37
NC_000008.9:g.19841257T= NCBI36
NG_008855.1:g.5396T=
NG_008855.2:g.42750T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.26T= MANE Select ENSP00000497642.1:p.Leu9=
ENST00000311322.8:c.26T= ENSP00000309757.6:p.Leu9=
ENST00000519773.1:c.26T= ENSP00000431028.1:p.Leu9=
ENST00000520959.5:c.-140-8714T= ENSP00000428496.1:n.-140-8714T=
ENST00000521994.1:n.211T=
ENST00000522701.5:c.26T= ENSP00000428557.1:p.Leu9=
ENST00000523696.1:n.95T=
ENST00000524029.5:c.26T= ENSP00000428237.1:p.Leu9=
NM_000237.2:c.26T= NP_000228.1:p.Leu9=
NM_000237.3:c.26T= MANE Select NP_000228.1:p.Leu9=