Canonical Allele Identifier: CA849549675

Gene: LPL

Linked Data

• dbSNP Id: rs1302566740
• gnomAD v3: 8-19939407-G-GC
• gnomAD v4: 8-19939407-G-GC
• MyVariant Identifiers: chr8:g.19796918_19796919insC (hg19) ; chr8:g.19939407_19939408insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19939409dup , CM000670.2:g.19939409dup	GRCh38
NC_000008.10:g.19796920dup , CM000670.1:g.19796920dup	GRCh37
NC_000008.9:g.19841200dup	NCBI36
NG_008855.1:g.5339dup
NG_008855.2:g.42693dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.-32dup MANE Select	ENSP00000497642.1:n.-32dup
ENST00000311322.8:c.-32dup	ENSP00000309757.6:n.-32dup
ENST00000519773.1:c.-32dup	ENSP00000431028.1:n.-32dup
ENST00000520959.5:c.-140-8771dup	ENSP00000428496.1:n.-140-8771dup
ENST00000521994.1:n.154dup
ENST00000522701.5:c.-32dup	ENSP00000428557.1:n.-32dup
ENST00000523696.1:n.38dup
ENST00000524029.5:c.-32dup	ENSP00000428237.1:n.-32dup
NM_000237.2:c.-32dup	NP_000228.1:n.-32dup
NM_000237.3:c.-32dup MANE Select	NP_000228.1:n.-32dup