Canonical Allele Identifier: CA370467690
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951905A>T , CM000670.2:g.19951905A>T GRCh38
NC_000008.10:g.19809416A>T , CM000670.1:g.19809416A>T GRCh37
NC_000008.9:g.19853696A>T NCBI36
NG_008855.1:g.17835A>T
NG_008855.2:g.55189A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.386A>T MANE Select ENSP00000497642.1:p.Lys129Ile
ENST00000311322.8:c.386A>T ENSP00000309757.6:p.Lys129Ile
ENST00000520959.5:c.158A>T ENSP00000428496.1:p.Lys53Ile
ENST00000524029.5:c.386A>T ENSP00000428237.1:p.Lys129Ile
NM_000237.2:c.386A>T NP_000228.1:p.Lys129Ile
NM_000237.3:c.386A>T MANE Select NP_000228.1:p.Lys129Ile