Canonical Allele Identifier: CA370467561

Gene: LPL

Linked Data

• gnomAD v4: 8-19951844-A-T
• MyVariant Identifiers: chr8:g.19809355A>T (hg19) ; chr8:g.19951844A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19951844A>T , CM000670.2:g.19951844A>T	GRCh38
NC_000008.10:g.19809355A>T , CM000670.1:g.19809355A>T	GRCh37
NC_000008.9:g.19853635A>T	NCBI36
NG_008855.1:g.17774A>T
NG_008855.2:g.55128A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.325A>T MANE Select	ENSP00000497642.1:p.Ile109Phe
ENST00000311322.8:c.325A>T	ENSP00000309757.6:p.Ile109Phe
ENST00000520959.5:c.97A>T	ENSP00000428496.1:p.Ile33Phe
ENST00000524029.5:c.325A>T	ENSP00000428237.1:p.Ile109Phe
NM_000237.2:c.325A>T	NP_000228.1:p.Ile109Phe
NM_000237.3:c.325A>T MANE Select	NP_000228.1:p.Ile109Phe