Canonical Allele Identifier: CA1769083448
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939413C= , CM000670.2:g.19939413C= GRCh38
NC_000008.10:g.19796924C= , CM000670.1:g.19796924C= GRCh37
NC_000008.9:g.19841204C= NCBI36
NG_008855.1:g.5343C=
NG_008855.2:g.42697C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.-28C= MANE Select ENSP00000497642.1:n.-28C=
ENST00000311322.8:c.-28C= ENSP00000309757.6:n.-28C=
ENST00000519773.1:c.-28C= ENSP00000431028.1:n.-28C=
ENST00000520959.5:c.-140-8767C= ENSP00000428496.1:n.-140-8767C=
ENST00000521994.1:n.158C=
ENST00000522701.5:c.-28C= ENSP00000428557.1:n.-28C=
ENST00000523696.1:n.42C=
ENST00000524029.5:c.-28C= ENSP00000428237.1:n.-28C=
NM_000237.2:c.-28C= NP_000228.1:n.-28C=
NM_000237.3:c.-28C= MANE Select NP_000228.1:n.-28C=