Canonical Allele Identifier: CA1769110605
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19960882T= , CM000670.2:g.19960882T= GRCh38
NC_000008.10:g.19818393T= , CM000670.1:g.19818393T= GRCh37
NC_000008.9:g.19862673T= NCBI36
NG_008855.1:g.26812T=
NG_008855.2:g.64166T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1140-19T= MANE Select ENSP00000497642.1:n.1140-19T=
ENST00000650478.1:c.80-19T= ENSP00000497560.1:n.80-19T=
ENST00000311322.8:c.1140-19T= ENSP00000309757.6:n.1140-19T=
NM_000237.2:c.1140-19T= NP_000228.1:n.1140-19T=
NM_000237.3:c.1140-19T= MANE Select NP_000228.1:n.1140-19T=