Canonical Allele Identifier: CA1769116754
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19967045G= , CM000670.2:g.19967045G= GRCh38
NC_000008.10:g.19824556G= , CM000670.1:g.19824556G= GRCh37
NC_000008.9:g.19868836G= NCBI36
NG_008855.1:g.32975G=
NG_008855.2:g.70329G=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.*1735G= MANE Select ENSP00000497642.1:n.*1735G=
ENST00000650478.1:c.2103G= ENSP00000497560.1:n.2103G=
ENST00000311322.8:c.*1735G= ENSP00000309757.6:n.*1735G=
NM_000237.2:c.*1735G= NP_000228.1:n.*1735G=
NM_000237.3:c.*1735G= MANE Select NP_000228.1:n.*1735G=