Canonical Allele Identifier: CA1769110391

Gene: LPL

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19960651_19960653delinsCTT , CM000670.2:g.19960651_19960653delinsCTT	GRCh38
NC_000008.10:g.19818162_19818164delinsCTT , CM000670.1:g.19818162_19818164delinsCTT	GRCh37
NC_000008.9:g.19862442_19862444delinsCTT	NCBI36
NG_008855.1:g.26581_26583delinsCTT
NG_008855.2:g.63935_63937delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.1140-250_1140-248delinsCTT MANE Select	ENSP00000497642.1:n.1140-250_1140-248delinsCTT
ENST00000650478.1:c.80-250_80-248delinsCTT	ENSP00000497560.1:n.80-250_80-248delinsCTT
ENST00000311322.8:c.1140-250_1140-248delinsCTT	ENSP00000309757.6:n.1140-250_1140-248delinsCTT
NM_000237.2:c.1140-250_1140-248delinsCTT	NP_000228.1:n.1140-250_1140-248delinsCTT
NM_000237.3:c.1140-250_1140-248delinsCTT MANE Select	NP_000228.1:n.1140-250_1140-248delinsCTT