Canonical Allele Identifier: CA1769117000
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19967230T= , CM000670.2:g.19967230T= GRCh38
NC_000008.10:g.19824741T= , CM000670.1:g.19824741T= GRCh37
NC_000008.9:g.19869021T= NCBI36
NG_008855.1:g.33160T=
NG_008855.2:g.70514T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.*1920T= MANE Select ENSP00000497642.1:n.*1920T=
ENST00000311322.8:c.*1920T= ENSP00000309757.6:n.*1920T=
NM_000237.2:c.*1920T= NP_000228.1:n.*1920T=
NM_000237.3:c.*1920T= MANE Select NP_000228.1:n.*1920T=