Canonical Allele Identifier: CA1769083200
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939271T= , CM000670.2:g.19939271T= GRCh38
NC_000008.10:g.19796782T= , CM000670.1:g.19796782T= GRCh37
NC_000008.9:g.19841062T= NCBI36
NG_008855.1:g.5201T=
NG_008855.2:g.42555T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.-170T= MANE Select ENSP00000497642.1:n.-170T=
ENST00000311322.8:c.-170T= ENSP00000309757.6:n.-170T=
ENST00000519773.1:c.-170T= ENSP00000431028.1:n.-170T=
ENST00000520959.5:c.-140-8909T= ENSP00000428496.1:n.-140-8909T=
ENST00000521994.1:n.16T=
ENST00000522701.5:c.-170T= ENSP00000428557.1:n.-170T=
ENST00000524029.5:c.-153-17T= ENSP00000428237.1:n.-153-17T=
NM_000237.2:c.-170T= NP_000228.1:n.-170T=
NM_000237.3:c.-170T= MANE Select NP_000228.1:n.-170T=