Canonical Allele Identifier: CA1769101641
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954024A= , CM000670.2:g.19954024A= GRCh38
NC_000008.10:g.19811535A= , CM000670.1:g.19811535A= GRCh37
NC_000008.9:g.19855815A= NCBI36
NG_008855.1:g.19954A=
NG_008855.2:g.57308A=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.542-96A= MANE Select ENSP00000497642.1:n.542-96A=
ENST00000311322.8:c.542-96A= ENSP00000309757.6:n.542-96A=
ENST00000520959.5:c.314-96A= ENSP00000428496.1:n.314-96A=
NM_000237.2:c.542-96A= NP_000228.1:n.542-96A=
NM_000237.3:c.542-96A= MANE Select NP_000228.1:n.542-96A=