Canonical Allele Identifier: CA2686360173

Gene: LPL

Linked Data

• gnomAD v4: 8-19952022-TCTTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19952026_19952029del , CM000670.2:g.19952026_19952029del	GRCh38
NC_000008.10:g.19809537_19809540del , CM000670.1:g.19809537_19809540del	GRCh37
NC_000008.9:g.19853817_19853820del	NCBI36
NG_008855.1:g.17956_17959del
NG_008855.2:g.55310_55313del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.429+78_429+81del MANE Select	ENSP00000497642.1:n.429+78_429+81del
ENST00000311322.8:c.429+78_429+81del	ENSP00000309757.6:n.429+78_429+81del
ENST00000520959.5:c.201+78_201+81del	ENSP00000428496.1:n.201+78_201+81del
NM_000237.2:c.429+78_429+81del	NP_000228.1:n.429+78_429+81del
NM_000237.3:c.429+78_429+81del MANE Select	NP_000228.1:n.429+78_429+81del