Canonical Allele Identifier: CA1769083464
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939422C= , CM000670.2:g.19939422C= GRCh38
NC_000008.10:g.19796933C= , CM000670.1:g.19796933C= GRCh37
NC_000008.9:g.19841213C= NCBI36
NG_008855.1:g.5352C=
NG_008855.2:g.42706C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.-19C= MANE Select ENSP00000497642.1:n.-19C=
ENST00000311322.8:c.-19C= ENSP00000309757.6:n.-19C=
ENST00000519773.1:c.-19C= ENSP00000431028.1:n.-19C=
ENST00000520959.5:c.-140-8758C= ENSP00000428496.1:n.-140-8758C=
ENST00000521994.1:n.167C=
ENST00000522701.5:c.-19C= ENSP00000428557.1:n.-19C=
ENST00000523696.1:n.51C=
ENST00000524029.5:c.-19C= ENSP00000428237.1:n.-19C=
NM_000237.2:c.-19C= NP_000228.1:n.-19C=
NM_000237.3:c.-19C= MANE Select NP_000228.1:n.-19C=