Canonical Allele Identifier: CA370638534
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19960907A>T , CM000670.2:g.19960907A>T GRCh38
NC_000008.10:g.19818418A>T , CM000670.1:g.19818418A>T GRCh37
NC_000008.9:g.19862698A>T NCBI36
NG_008855.1:g.26837A>T
NG_008855.2:g.64191A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1146A>T MANE Select ENSP00000497642.1:p.Glu382Asp
ENST00000650478.1:c.86A>T ENSP00000497560.1:p.Lys29Met
ENST00000311322.8:c.1146A>T ENSP00000309757.6:p.Glu382Asp
NM_000237.2:c.1146A>T NP_000228.1:p.Glu382Asp
NM_000237.3:c.1146A>T MANE Select NP_000228.1:p.Glu382Asp