Canonical Allele Identifier: CA652074988
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939432_19939433insT , CM000670.2:g.19939432_19939433insT GRCh38
NC_000008.10:g.19796943_19796944insT , CM000670.1:g.19796943_19796944insT GRCh37
NC_000008.9:g.19841223_19841224insT NCBI36
NG_008855.1:g.5362_5363insT
NG_008855.2:g.42716_42717insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.-9_-8insT MANE Select ENSP00000497642.1:n.-9_-8insT
ENST00000311322.8:c.-9_-8insT ENSP00000309757.6:n.-9_-8insT
ENST00000519773.1:c.-9_-8insT ENSP00000431028.1:n.-9_-8insT
ENST00000520959.5:c.-140-8748_-140-8747insT ENSP00000428496.1:n.-140-8748_-140-8747insT
ENST00000521994.1:n.177_178insT
ENST00000522701.5:c.-9_-8insT ENSP00000428557.1:n.-9_-8insT
ENST00000523696.1:n.61_62insT
ENST00000524029.5:c.-9_-8insT ENSP00000428237.1:n.-9_-8insT
NM_000237.2:c.-9_-8insT NP_000228.1:n.-9_-8insT
NM_000237.3:c.-9_-8insT MANE Select NP_000228.1:n.-9_-8insT