Canonical Allele Identifier: CA4655260

Gene: LPL

Linked Data

• ClinVar Variation Id: 1095681
• ClinVar RCV Id: RCV001416679
• dbSNP Id: rs554223627
• ExAC: 8:19796966 C / A
• gnomAD v2: 8-19796966-C-A
• gnomAD v3: 8-19939455-C-A
• gnomAD v4: 8-19939455-C-A
• COSMIC: COSM2785093
• MyVariant Identifiers: chr8:g.19796966C>A (hg19) ; chr8:g.19939455C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19939455C>A , CM000670.2:g.19939455C>A	GRCh38
NC_000008.10:g.19796966C>A , CM000670.1:g.19796966C>A	GRCh37
NC_000008.9:g.19841246C>A	NCBI36
NG_008855.1:g.5385C>A
NG_008855.2:g.42739C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.15C>A MANE Select	ENSP00000497642.1:p.Ala5=
ENST00000311322.8:c.15C>A	ENSP00000309757.6:p.Ala5=
ENST00000519773.1:c.15C>A	ENSP00000431028.1:p.Ala5=
ENST00000520959.5:c.-140-8725C>A	ENSP00000428496.1:n.-140-8725C>A
ENST00000521994.1:n.200C>A
ENST00000522701.5:c.15C>A	ENSP00000428557.1:p.Ala5=
ENST00000523696.1:n.84C>A
ENST00000524029.5:c.15C>A	ENSP00000428237.1:p.Ala5=
NM_000237.2:c.15C>A	NP_000228.1:p.Ala5=
NM_000237.3:c.15C>A MANE Select	NP_000228.1:p.Ala5=