Canonical Allele Identifier: CA1769104713
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19956005G= , CM000670.2:g.19956005G= GRCh38
NC_000008.10:g.19813516G= , CM000670.1:g.19813516G= GRCh37
NC_000008.9:g.19857796G= NCBI36
NG_008855.1:g.21935G=
NG_008855.2:g.59289G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.940G= MANE Select ENSP00000497642.1:p.Gly314=
ENST00000650478.1:c.1G= ENSP00000497560.1:p.Gly1=
ENST00000311322.8:c.940G= ENSP00000309757.6:p.Gly314=
NM_000237.2:c.940G= NP_000228.1:p.Gly314=
NM_000237.3:c.940G= MANE Select NP_000228.1:p.Gly314=