Canonical Allele Identifier: CA173618776
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs386723272

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19967156_19967158delinsTAA , CM000670.2:g.19967156_19967158delinsTAA GRCh38
NC_000008.10:g.19824667_19824669delinsTAA , CM000670.1:g.19824667_19824669delinsTAA GRCh37
NC_000008.9:g.19868947_19868949delinsTAA NCBI36
NG_008855.1:g.33086_33088delinsTAA
NG_008855.2:g.70440_70442delinsTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.*1846_*1848delinsTAA MANE Select ENSP00000497642.1:n.*1846_*1848delinsTAA
ENST00000650478.1:c.2214_2216delinsTAA ENSP00000497560.1:n.2214_2216delinsTAA
ENST00000311322.8:c.*1846_*1848delinsTAA ENSP00000309757.6:n.*1846_*1848delinsTAA
NM_000237.2:c.*1846_*1848delinsTAA NP_000228.1:n.*1846_*1848delinsTAA
NM_000237.3:c.*1846_*1848delinsTAA MANE Select NP_000228.1:n.*1846_*1848delinsTAA