Canonical Allele Identifier: CA173379096

Gene: LPL

Linked Data

• dbSNP Id: rs1003344641
• MyVariant Identifiers: chr8:g.19815454G>A (hg19) ; chr8:g.19957943G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19957943G>A , CM000670.2:g.19957943G>A	GRCh38
NC_000008.10:g.19815454G>A , CM000670.1:g.19815454G>A	GRCh37
NC_000008.9:g.19859734G>A	NCBI36
NG_008855.1:g.23873G>A
NG_008855.2:g.61227G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.1019-1317G>A MANE Select	ENSP00000497642.1:n.1019-1317G>A
ENST00000650478.1:c.79+1860G>A	ENSP00000497560.1:n.79+1860G>A
ENST00000311322.8:c.1019-1317G>A	ENSP00000309757.6:n.1019-1317G>A
NM_000237.2:c.1019-1317G>A	NP_000228.1:n.1019-1317G>A
NM_000237.3:c.1019-1317G>A MANE Select	NP_000228.1:n.1019-1317G>A