Canonical Allele Identifier: CA2779304280
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19953985G>T , CM000670.2:g.19953985G>T GRCh38
NC_000008.10:g.19811496G>T , CM000670.1:g.19811496G>T GRCh37
NC_000008.9:g.19855776G>T NCBI36
NG_008855.1:g.19915G>T
NG_008855.2:g.57269G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.542-135G>T MANE Select ENSP00000497642.1:n.542-135G>T
ENST00000311322.8:c.542-135G>T ENSP00000309757.6:n.542-135G>T
ENST00000520959.5:c.314-135G>T ENSP00000428496.1:n.314-135G>T
NM_000237.2:c.542-135G>T NP_000228.1:n.542-135G>T
NM_000237.3:c.542-135G>T MANE Select NP_000228.1:n.542-135G>T