Canonical Allele Identifier: CA459678558

Gene: LPL

Linked Data

• dbSNP Id: rs1375340436
• MyVariant Identifiers: chr8:g.19809450C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19951939C>T , CM000670.2:g.19951939C>T	GRCh38
NC_000008.10:g.19809450C>T , CM000670.1:g.19809450C>T	GRCh37
NC_000008.9:g.19853730C>T	NCBI36
NG_008855.1:g.17869C>T
NG_008855.2:g.55223C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.420C>T MANE Select	ENSP00000497642.1:p.Asn140=
ENST00000311322.8:c.420C>T	ENSP00000309757.6:p.Asn140=
ENST00000520959.5:c.192C>T	ENSP00000428496.1:p.Asn64=
NM_000237.2:c.420C>T	NP_000228.1:p.Asn140=
NM_000237.3:c.420C>T MANE Select	NP_000228.1:p.Asn140=