Canonical Allele Identifier: CA1769098149

Gene: LPL

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19952022_19952027delinsTCTTCC , CM000670.2:g.19952022_19952027delinsTCTTCC	GRCh38
NC_000008.10:g.19809533_19809538delinsTCTTCC , CM000670.1:g.19809533_19809538delinsTCTTCC	GRCh37
NC_000008.9:g.19853813_19853818delinsTCTTCC	NCBI36
NG_008855.1:g.17952_17957delinsTCTTCC
NG_008855.2:g.55306_55311delinsTCTTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.429+74_429+79delinsTCTTCC MANE Select	ENSP00000497642.1:n.429+74_429+79delinsTCTTCC
ENST00000311322.8:c.429+74_429+79delinsTCTTCC	ENSP00000309757.6:n.429+74_429+79delinsTCTTCC
ENST00000520959.5:c.201+74_201+79delinsTCTTCC	ENSP00000428496.1:n.201+74_201+79delinsTCTTCC
NM_000237.2:c.429+74_429+79delinsTCTTCC	NP_000228.1:n.429+74_429+79delinsTCTTCC
NM_000237.3:c.429+74_429+79delinsTCTTCC MANE Select	NP_000228.1:n.429+74_429+79delinsTCTTCC