Canonical Allele Identifier: CA2686357390
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939344_19939348del , CM000670.2:g.19939344_19939348del GRCh38
NC_000008.10:g.19796855_19796859del , CM000670.1:g.19796855_19796859del GRCh37
NC_000008.9:g.19841135_19841139del NCBI36
NG_008855.1:g.5274_5278del
NG_008855.2:g.42628_42632del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.-97_-93del MANE Select ENSP00000497642.1:n.-97_-93del
ENST00000311322.8:c.-97_-93del ENSP00000309757.6:n.-97_-93del
ENST00000519773.1:c.-97_-93del ENSP00000431028.1:n.-97_-93del
ENST00000520959.5:c.-140-8836_-140-8832del ENSP00000428496.1:n.-140-8836_-140-8832del
ENST00000521994.1:n.89_93del
ENST00000522701.5:c.-97_-93del ENSP00000428557.1:n.-97_-93del
ENST00000524029.5:c.-97_-93del ENSP00000428237.1:n.-97_-93del
NM_000237.2:c.-97_-93del NP_000228.1:n.-97_-93del
NM_000237.3:c.-97_-93del MANE Select NP_000228.1:n.-97_-93del