Canonical Allele Identifier: CA1769083379
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939387C= , CM000670.2:g.19939387C= GRCh38
NC_000008.10:g.19796898C= , CM000670.1:g.19796898C= GRCh37
NC_000008.9:g.19841178C= NCBI36
NG_008855.1:g.5317C=
NG_008855.2:g.42671C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.-54C= MANE Select ENSP00000497642.1:n.-54C=
ENST00000311322.8:c.-54C= ENSP00000309757.6:n.-54C=
ENST00000519773.1:c.-54C= ENSP00000431028.1:n.-54C=
ENST00000520959.5:c.-140-8793C= ENSP00000428496.1:n.-140-8793C=
ENST00000521994.1:n.132C=
ENST00000522701.5:c.-54C= ENSP00000428557.1:n.-54C=
ENST00000523696.1:n.16C=
ENST00000524029.5:c.-54C= ENSP00000428237.1:n.-54C=
NM_000237.2:c.-54C= NP_000228.1:n.-54C=
NM_000237.3:c.-54C= MANE Select NP_000228.1:n.-54C=