Canonical Allele Identifier: CA370468509
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954245A>T , CM000670.2:g.19954245A>T GRCh38
NC_000008.10:g.19811756A>T , CM000670.1:g.19811756A>T GRCh37
NC_000008.9:g.19856036A>T NCBI36
NG_008855.1:g.20175A>T
NG_008855.2:g.57529A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.667A>T MANE Select ENSP00000497642.1:p.Ile223Phe
ENST00000311322.8:c.667A>T ENSP00000309757.6:p.Ile223Phe
NM_000237.2:c.667A>T NP_000228.1:p.Ile223Phe
NM_000237.3:c.667A>T MANE Select NP_000228.1:p.Ile223Phe