Canonical Allele Identifier: CA849561554

Gene: LPL

Linked Data

• dbSNP Id: rs1405976493
• MyVariant Identifiers: chr8:g.19815277_19815278del (hg19) ; chr8:g.19957766_19957767del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19957769_19957770del , CM000670.2:g.19957769_19957770del	GRCh38
NC_000008.10:g.19815280_19815281del , CM000670.1:g.19815280_19815281del	GRCh37
NC_000008.9:g.19859560_19859561del	NCBI36
NG_008855.1:g.23699_23700del
NG_008855.2:g.61053_61054del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.1019-1491_1019-1490del MANE Select	ENSP00000497642.1:n.1019-1491_1019-1490del
ENST00000650478.1:c.79+1686_79+1687del	ENSP00000497560.1:n.79+1686_79+1687del
ENST00000311322.8:c.1019-1491_1019-1490del	ENSP00000309757.6:n.1019-1491_1019-1490del
NM_000237.2:c.1019-1491_1019-1490del	NP_000228.1:n.1019-1491_1019-1490del
NM_000237.3:c.1019-1491_1019-1490del MANE Select	NP_000228.1:n.1019-1491_1019-1490del