Canonical Allele Identifier: CA1769083544
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939462G= , CM000670.2:g.19939462G= GRCh38
NC_000008.10:g.19796973G= , CM000670.1:g.19796973G= GRCh37
NC_000008.9:g.19841253G= NCBI36
NG_008855.1:g.5392G=
NG_008855.2:g.42746G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.22G= MANE Select ENSP00000497642.1:p.Val8=
ENST00000311322.8:c.22G= ENSP00000309757.6:p.Val8=
ENST00000519773.1:c.22G= ENSP00000431028.1:p.Val8=
ENST00000520959.5:c.-140-8718G= ENSP00000428496.1:n.-140-8718G=
ENST00000521994.1:n.207G=
ENST00000522701.5:c.22G= ENSP00000428557.1:p.Val8=
ENST00000523696.1:n.91G=
ENST00000524029.5:c.22G= ENSP00000428237.1:p.Val8=
NM_000237.2:c.22G= NP_000228.1:p.Val8=
NM_000237.3:c.22G= MANE Select NP_000228.1:p.Val8=