Canonical Allele Identifier: CA1769104649
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955942T= , CM000670.2:g.19955942T= GRCh38
NC_000008.10:g.19813453T= , CM000670.1:g.19813453T= GRCh37
NC_000008.9:g.19857733T= NCBI36
NG_008855.1:g.21872T=
NG_008855.2:g.59226T=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.877T= MANE Select ENSP00000497642.1:p.Ser293=
ENST00000311322.8:c.877T= ENSP00000309757.6:p.Ser293=
NM_000237.2:c.877T= NP_000228.1:p.Ser293=
NM_000237.3:c.877T= MANE Select NP_000228.1:p.Ser293=