Canonical Allele Identifier: CA1769101551
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19953958G= , CM000670.2:g.19953958G= GRCh38
NC_000008.10:g.19811469G= , CM000670.1:g.19811469G= GRCh37
NC_000008.9:g.19855749G= NCBI36
NG_008855.1:g.19888G=
NG_008855.2:g.57242G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.542-162G= MANE Select ENSP00000497642.1:n.542-162G=
ENST00000311322.8:c.542-162G= ENSP00000309757.6:n.542-162G=
ENST00000520959.5:c.314-162G= ENSP00000428496.1:n.314-162G=
NM_000237.2:c.542-162G= NP_000228.1:n.542-162G=
NM_000237.3:c.542-162G= MANE Select NP_000228.1:n.542-162G=