Canonical Allele Identifier: CA580154251

Gene: LPL

Linked Data

• dbSNP Id: rs1563561465
• gnomAD v2: 8-19796944-G-C
• gnomAD v4: 8-19939433-G-C
• MyVariant Identifiers: chr8:g.19796944_19796946delinsCCC (hg19) ; chr8:g.19939433_19939435delinsCCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19939433G>C , CM000670.2:g.19939433G>C	GRCh38
NC_000008.10:g.19796944G>C , CM000670.1:g.19796944G>C	GRCh37
NC_000008.9:g.19841224G>C	NCBI36
NG_008855.1:g.5363G>C
NG_008855.2:g.42717G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.-8G>C MANE Select	ENSP00000497642.1:n.-8G>C
ENST00000311322.8:c.-8G>C	ENSP00000309757.6:n.-8G>C
ENST00000519773.1:c.-8G>C	ENSP00000431028.1:n.-8G>C
ENST00000520959.5:c.-140-8747G>C	ENSP00000428496.1:n.-140-8747G>C
ENST00000521994.1:n.178G>C
ENST00000522701.5:c.-8G>C	ENSP00000428557.1:n.-8G>C
ENST00000523696.1:n.62G>C
ENST00000524029.5:c.-8G>C	ENSP00000428237.1:n.-8G>C
NM_000237.2:c.-8G>C	NP_000228.1:n.-8G>C
NM_000237.3:c.-8G>C MANE Select	NP_000228.1:n.-8G>C