Canonical Allele Identifier: CA370469150

Gene: LPL

Linked Data

• MyVariant Identifiers: chr8:g.19813453T>G (hg19) ; chr8:g.19955942T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19955942T>G , CM000670.2:g.19955942T>G	GRCh38
NC_000008.10:g.19813453T>G , CM000670.1:g.19813453T>G	GRCh37
NC_000008.9:g.19857733T>G	NCBI36
NG_008855.1:g.21872T>G
NG_008855.2:g.59226T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000650287.1:c.877T>G MANE Select	ENSP00000497642.1:p.Ser293Ala
ENST00000311322.8:c.877T>G	ENSP00000309757.6:p.Ser293Ala
NM_000237.2:c.877T>G	NP_000228.1:p.Ser293Ala
NM_000237.3:c.877T>G MANE Select	NP_000228.1:p.Ser293Ala