Canonical Allele Identifier: CA173376190

Gene: LPL

Linked Data

• dbSNP Id: rs78577362
• MyVariant Identifiers: chr8:g.19809053A>T (hg19) ; chr8:g.19951542A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19951542A>T , CM000670.2:g.19951542A>T	GRCh38
NC_000008.10:g.19809053A>T , CM000670.1:g.19809053A>T	GRCh37
NC_000008.9:g.19853333A>T	NCBI36
NG_008855.1:g.17472A>T
NG_008855.2:g.54826A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.250-227A>T MANE Select	ENSP00000497642.1:n.250-227A>T
ENST00000311322.8:c.250-227A>T	ENSP00000309757.6:n.250-227A>T
ENST00000520959.5:c.22-227A>T	ENSP00000428496.1:n.22-227A>T
ENST00000521994.1:n.435-155A>T
ENST00000522701.5:c.250-227A>T	ENSP00000428557.1:n.250-227A>T
ENST00000524029.5:c.250-227A>T	ENSP00000428237.1:n.250-227A>T
NM_000237.2:c.250-227A>T	NP_000228.1:n.250-227A>T
NM_000237.3:c.250-227A>T MANE Select	NP_000228.1:n.250-227A>T