Canonical Allele Identifier: CA1769116598
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19966857T= , CM000670.2:g.19966857T= GRCh38
NC_000008.10:g.19824368T= , CM000670.1:g.19824368T= GRCh37
NC_000008.9:g.19868648T= NCBI36
NG_008855.1:g.32787T=
NG_008855.2:g.70141T=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.*1547T= MANE Select ENSP00000497642.1:n.*1547T=
ENST00000650478.1:c.1915T= ENSP00000497560.1:n.1915T=
ENST00000311322.8:c.*1547T= ENSP00000309757.6:n.*1547T=
NM_000237.2:c.*1547T= NP_000228.1:n.*1547T=
NM_000237.3:c.*1547T= MANE Select NP_000228.1:n.*1547T=