Canonical Allele Identifier: CA459719174

Gene: LPL

Linked Data

• MyVariant Identifiers: chr8:g.19818478A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19960967A>C , CM000670.2:g.19960967A>C	GRCh38
NC_000008.10:g.19818478A>C , CM000670.1:g.19818478A>C	GRCh37
NC_000008.9:g.19862758A>C	NCBI36
NG_008855.1:g.26897A>C
NG_008855.2:g.64251A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.1206A>C MANE Select	ENSP00000497642.1:p.Leu402=
ENST00000650478.1:c.146A>C	ENSP00000497560.1:n.146A>C
ENST00000311322.8:c.1206A>C	ENSP00000309757.6:p.Leu402=
NM_000237.2:c.1206A>C	NP_000228.1:p.Leu402=
NM_000237.3:c.1206A>C MANE Select	NP_000228.1:p.Leu402=