Canonical Allele Identifier: CA1769101602
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19953990C= , CM000670.2:g.19953990C= GRCh38
NC_000008.10:g.19811501C= , CM000670.1:g.19811501C= GRCh37
NC_000008.9:g.19855781C= NCBI36
NG_008855.1:g.19920C=
NG_008855.2:g.57274C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.542-130C= MANE Select ENSP00000497642.1:n.542-130C=
ENST00000311322.8:c.542-130C= ENSP00000309757.6:n.542-130C=
ENST00000520959.5:c.314-130C= ENSP00000428496.1:n.314-130C=
NM_000237.2:c.542-130C= NP_000228.1:n.542-130C=
NM_000237.3:c.542-130C= MANE Select NP_000228.1:n.542-130C=