Canonical Allele Identifier: CA580154224

Gene: LPL

Linked Data

• dbSNP Id: rs1227105676
• gnomAD v2: 8-19796910-C-G
• gnomAD v4: 8-19939399-C-G
• MyVariant Identifiers: chr8:g.19796910C>G (hg19) ; chr8:g.19939399C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19939399C>G , CM000670.2:g.19939399C>G	GRCh38
NC_000008.10:g.19796910C>G , CM000670.1:g.19796910C>G	GRCh37
NC_000008.9:g.19841190C>G	NCBI36
NG_008855.1:g.5329C>G
NG_008855.2:g.42683C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.-42C>G MANE Select	ENSP00000497642.1:n.-42C>G
ENST00000311322.8:c.-42C>G	ENSP00000309757.6:n.-42C>G
ENST00000519773.1:c.-42C>G	ENSP00000431028.1:n.-42C>G
ENST00000520959.5:c.-140-8781C>G	ENSP00000428496.1:n.-140-8781C>G
ENST00000521994.1:n.144C>G
ENST00000522701.5:c.-42C>G	ENSP00000428557.1:n.-42C>G
ENST00000523696.1:n.28C>G
ENST00000524029.5:c.-42C>G	ENSP00000428237.1:n.-42C>G
NM_000237.2:c.-42C>G	NP_000228.1:n.-42C>G
NM_000237.3:c.-42C>G MANE Select	NP_000228.1:n.-42C>G