Canonical Allele Identifier: CA370468428

Gene: LPL

Linked Data

• MyVariant Identifiers: chr8:g.19811715T>C (hg19) ; chr8:g.19954204T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19954204T>C , CM000670.2:g.19954204T>C	GRCh38
NC_000008.10:g.19811715T>C , CM000670.1:g.19811715T>C	GRCh37
NC_000008.9:g.19855995T>C	NCBI36
NG_008855.1:g.20134T>C
NG_008855.2:g.57488T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000650287.1:c.626T>C MANE Select	ENSP00000497642.1:p.Leu209Ser
ENST00000311322.8:c.626T>C	ENSP00000309757.6:p.Leu209Ser
NM_000237.2:c.626T>C	NP_000228.1:p.Leu209Ser
NM_000237.3:c.626T>C MANE Select	NP_000228.1:p.Leu209Ser