Canonical Allele Identifier: CA1769083395
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939390C= , CM000670.2:g.19939390C= GRCh38
NC_000008.10:g.19796901C= , CM000670.1:g.19796901C= GRCh37
NC_000008.9:g.19841181C= NCBI36
NG_008855.1:g.5320C=
NG_008855.2:g.42674C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.-51C= MANE Select ENSP00000497642.1:n.-51C=
ENST00000311322.8:c.-51C= ENSP00000309757.6:n.-51C=
ENST00000519773.1:c.-51C= ENSP00000431028.1:n.-51C=
ENST00000520959.5:c.-140-8790C= ENSP00000428496.1:n.-140-8790C=
ENST00000521994.1:n.135C=
ENST00000522701.5:c.-51C= ENSP00000428557.1:n.-51C=
ENST00000523696.1:n.19C=
ENST00000524029.5:c.-51C= ENSP00000428237.1:n.-51C=
NM_000237.2:c.-51C= NP_000228.1:n.-51C=
NM_000237.3:c.-51C= MANE Select NP_000228.1:n.-51C=