Canonical Allele Identifier: CA370638521

Gene: LPL

Linked Data

• gnomAD v4: 8-19960902-C-A
• MyVariant Identifiers: chr8:g.19818413C>A (hg19) ; chr8:g.19960902C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19960902C>A , CM000670.2:g.19960902C>A	GRCh38
NC_000008.10:g.19818413C>A , CM000670.1:g.19818413C>A	GRCh37
NC_000008.9:g.19862693C>A	NCBI36
NG_008855.1:g.26832C>A
NG_008855.2:g.64186C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.1141C>A MANE Select	ENSP00000497642.1:p.Pro381Thr
ENST00000650478.1:c.81C>A	ENSP00000497560.1:p.Gly27=
ENST00000311322.8:c.1141C>A	ENSP00000309757.6:p.Pro381Thr
NM_000237.2:c.1141C>A	NP_000228.1:p.Pro381Thr
NM_000237.3:c.1141C>A MANE Select	NP_000228.1:p.Pro381Thr