Canonical Allele Identifier: CA1769097762
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951862T= , CM000670.2:g.19951862T= GRCh38
NC_000008.10:g.19809373T= , CM000670.1:g.19809373T= GRCh37
NC_000008.9:g.19853653T= NCBI36
NG_008855.1:g.17792T=
NG_008855.2:g.55146T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.343T= MANE Select ENSP00000497642.1:p.Ser115=
ENST00000311322.8:c.343T= ENSP00000309757.6:p.Ser115=
ENST00000520959.5:c.115T= ENSP00000428496.1:p.Ser39=
ENST00000524029.5:c.343T= ENSP00000428237.1:p.Ser115=
NM_000237.2:c.343T= NP_000228.1:p.Ser115=
NM_000237.3:c.343T= MANE Select NP_000228.1:p.Ser115=