Canonical Allele Identifier: CA370468940

Gene: LPL

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.782A>T MANE Select	ENSP00000497642.1:p.Asp261Val
ENST00000311322.8:c.782A>T	ENSP00000309757.6:p.Asp261Val
NM_000237.2:c.782A>T	NP_000228.1:p.Asp261Val
NM_000237.3:c.782A>T MANE Select	NP_000228.1:p.Asp261Val