Canonical Allele Identifier: CA370468291
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954138C>T , CM000670.2:g.19954138C>T GRCh38
NC_000008.10:g.19811649C>T , CM000670.1:g.19811649C>T GRCh37
NC_000008.9:g.19855929C>T NCBI36
NG_008855.1:g.20068C>T
NG_008855.2:g.57422C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.560C>T MANE Select ENSP00000497642.1:p.Pro187Leu
ENST00000311322.8:c.560C>T ENSP00000309757.6:p.Pro187Leu
ENST00000520959.5:c.332C>T ENSP00000428496.1:p.Pro111Leu
NM_000237.2:c.560C>T NP_000228.1:p.Pro187Leu
NM_000237.3:c.560C>T MANE Select NP_000228.1:p.Pro187Leu