Canonical Allele Identifier: CA1769110630
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19960902C= , CM000670.2:g.19960902C= GRCh38
NC_000008.10:g.19818413C= , CM000670.1:g.19818413C= GRCh37
NC_000008.9:g.19862693C= NCBI36
NG_008855.1:g.26832C=
NG_008855.2:g.64186C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1141C= MANE Select ENSP00000497642.1:p.Pro381=
ENST00000650478.1:c.81C= ENSP00000497560.1:p.Gly27=
ENST00000311322.8:c.1141C= ENSP00000309757.6:p.Pro381=
NM_000237.2:c.1141C= NP_000228.1:p.Pro381=
NM_000237.3:c.1141C= MANE Select NP_000228.1:p.Pro381=