Canonical Allele Identifier: CA1769083417
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939400G= , CM000670.2:g.19939400G= GRCh38
NC_000008.10:g.19796911G= , CM000670.1:g.19796911G= GRCh37
NC_000008.9:g.19841191G= NCBI36
NG_008855.1:g.5330G=
NG_008855.2:g.42684G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.-41G= MANE Select ENSP00000497642.1:n.-41G=
ENST00000311322.8:c.-41G= ENSP00000309757.6:n.-41G=
ENST00000519773.1:c.-41G= ENSP00000431028.1:n.-41G=
ENST00000520959.5:c.-140-8780G= ENSP00000428496.1:n.-140-8780G=
ENST00000521994.1:n.145G=
ENST00000522701.5:c.-41G= ENSP00000428557.1:n.-41G=
ENST00000523696.1:n.29G=
ENST00000524029.5:c.-41G= ENSP00000428237.1:n.-41G=
NM_000237.2:c.-41G= NP_000228.1:n.-41G=
NM_000237.3:c.-41G= MANE Select NP_000228.1:n.-41G=