Canonical Allele Identifier: CA918215073

Gene: LPL

Linked Data

• dbSNP Id: rs1563561301

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19939375_19939381del , CM000670.2:g.19939375_19939381del	GRCh38
NC_000008.10:g.19796886_19796892del , CM000670.1:g.19796886_19796892del	GRCh37
NC_000008.9:g.19841166_19841172del	NCBI36
NG_008855.1:g.5305_5311del
NG_008855.2:g.42659_42665del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.-66_-60del MANE Select	ENSP00000497642.1:n.-66_-60del
ENST00000311322.8:c.-66_-60del	ENSP00000309757.6:n.-66_-60del
ENST00000519773.1:c.-66_-60del	ENSP00000431028.1:n.-66_-60del
ENST00000520959.5:c.-140-8805_-140-8799del	ENSP00000428496.1:n.-140-8805_-140-8799del
ENST00000521994.1:n.120_126del
ENST00000522701.5:c.-66_-60del	ENSP00000428557.1:n.-66_-60del
ENST00000523696.1:n.4_10del
ENST00000524029.5:c.-66_-60del	ENSP00000428237.1:n.-66_-60del
NM_000237.2:c.-66_-60del	NP_000228.1:n.-66_-60del
NM_000237.3:c.-66_-60del MANE Select	NP_000228.1:n.-66_-60del