Canonical Allele Identifier: CA1769104155
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955535G= , CM000670.2:g.19955535G= GRCh38
NC_000008.10:g.19813046G= , CM000670.1:g.19813046G= GRCh37
NC_000008.9:g.19857326G= NCBI36
NG_008855.1:g.21465G=
NG_008855.2:g.58819G=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.776-306G= MANE Select ENSP00000497642.1:n.776-306G=
ENST00000311322.8:c.776-306G= ENSP00000309757.6:n.776-306G=
NM_000237.2:c.776-306G= NP_000228.1:n.776-306G=
NM_000237.3:c.776-306G= MANE Select NP_000228.1:n.776-306G=