Canonical Allele Identifier: CA1769103157
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954530T= , CM000670.2:g.19954530T= GRCh38
NC_000008.10:g.19812041T= , CM000670.1:g.19812041T= GRCh37
NC_000008.9:g.19856321T= NCBI36
NG_008855.1:g.20460T=
NG_008855.2:g.57814T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.775+177T= MANE Select ENSP00000497642.1:n.775+177T=
ENST00000311322.8:c.775+177T= ENSP00000309757.6:n.775+177T=
NM_000237.2:c.775+177T= NP_000228.1:n.775+177T=
NM_000237.3:c.775+177T= MANE Select NP_000228.1:n.775+177T=