Canonical Allele Identifier: CA1769101658
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954029T= , CM000670.2:g.19954029T= GRCh38
NC_000008.10:g.19811540T= , CM000670.1:g.19811540T= GRCh37
NC_000008.9:g.19855820T= NCBI36
NG_008855.1:g.19959T=
NG_008855.2:g.57313T=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.542-91T= MANE Select ENSP00000497642.1:n.542-91T=
ENST00000311322.8:c.542-91T= ENSP00000309757.6:n.542-91T=
ENST00000520959.5:c.314-91T= ENSP00000428496.1:n.314-91T=
NM_000237.2:c.542-91T= NP_000228.1:n.542-91T=
NM_000237.3:c.542-91T= MANE Select NP_000228.1:n.542-91T=