Canonical Allele Identifier: CA459879312

Gene: LPL

Linked Data

• MyVariant Identifiers: chr8:g.19811647A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19954136A>T , CM000670.2:g.19954136A>T	GRCh38
NC_000008.10:g.19811647A>T , CM000670.1:g.19811647A>T	GRCh37
NC_000008.9:g.19855927A>T	NCBI36
NG_008855.1:g.20066A>T
NG_008855.2:g.57420A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000650287.1:c.558A>T MANE Select	ENSP00000497642.1:p.Gly186=
ENST00000311322.8:c.558A>T	ENSP00000309757.6:p.Gly186=
ENST00000520959.5:c.330A>T	ENSP00000428496.1:p.Gly110=
NM_000237.2:c.558A>T	NP_000228.1:p.Gly186=
NM_000237.3:c.558A>T MANE Select	NP_000228.1:p.Gly186=