Canonical Allele Identifier: CA370468606
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954290A>G , CM000670.2:g.19954290A>G GRCh38
NC_000008.10:g.19811801A>G , CM000670.1:g.19811801A>G GRCh37
NC_000008.9:g.19856081A>G NCBI36
NG_008855.1:g.20220A>G
NG_008855.2:g.57574A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.712A>G MANE Select ENSP00000497642.1:p.Thr238Ala
ENST00000311322.8:c.712A>G ENSP00000309757.6:p.Thr238Ala
NM_000237.2:c.712A>G NP_000228.1:p.Thr238Ala
NM_000237.3:c.712A>G MANE Select NP_000228.1:p.Thr238Ala