Canonical Allele Identifier: CA370468939

Gene: LPL

Linked Data

• MyVariant Identifiers: chr8:g.19813358A>G (hg19) ; chr8:g.19955847A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19955847A>G , CM000670.2:g.19955847A>G	GRCh38
NC_000008.10:g.19813358A>G , CM000670.1:g.19813358A>G	GRCh37
NC_000008.9:g.19857638A>G	NCBI36
NG_008855.1:g.21777A>G
NG_008855.2:g.59131A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000650287.1:c.782A>G MANE Select	ENSP00000497642.1:p.Asp261Gly
ENST00000311322.8:c.782A>G	ENSP00000309757.6:p.Asp261Gly
NM_000237.2:c.782A>G	NP_000228.1:p.Asp261Gly
NM_000237.3:c.782A>G MANE Select	NP_000228.1:p.Asp261Gly