Canonical Allele Identifier: CA1769101796
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954101T= , CM000670.2:g.19954101T= GRCh38
NC_000008.10:g.19811612T= , CM000670.1:g.19811612T= GRCh37
NC_000008.9:g.19855892T= NCBI36
NG_008855.1:g.20031T=
NG_008855.2:g.57385T=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.542-19T= MANE Select ENSP00000497642.1:n.542-19T=
ENST00000311322.8:c.542-19T= ENSP00000309757.6:n.542-19T=
ENST00000520959.5:c.314-19T= ENSP00000428496.1:n.314-19T=
NM_000237.2:c.542-19T= NP_000228.1:n.542-19T=
NM_000237.3:c.542-19T= MANE Select NP_000228.1:n.542-19T=