Canonical Allele Identifier: CA1769101592
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19953975T= , CM000670.2:g.19953975T= GRCh38
NC_000008.10:g.19811486T= , CM000670.1:g.19811486T= GRCh37
NC_000008.9:g.19855766T= NCBI36
NG_008855.1:g.19905T=
NG_008855.2:g.57259T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.542-145T= MANE Select ENSP00000497642.1:n.542-145T=
ENST00000311322.8:c.542-145T= ENSP00000309757.6:n.542-145T=
ENST00000520959.5:c.314-145T= ENSP00000428496.1:n.314-145T=
NM_000237.2:c.542-145T= NP_000228.1:n.542-145T=
NM_000237.3:c.542-145T= MANE Select NP_000228.1:n.542-145T=