Canonical Allele Identifier: CA1769112363
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19962771T= , CM000670.2:g.19962771T= GRCh38
NC_000008.10:g.19820282T= , CM000670.1:g.19820282T= GRCh37
NC_000008.9:g.19864562T= NCBI36
NG_008855.1:g.28701T=
NG_008855.2:g.66055T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1427+552T= MANE Select ENSP00000497642.1:n.1427+552T=
ENST00000650478.1:c.367+552T= ENSP00000497560.1:n.367+552T=
ENST00000311322.8:c.1427+552T= ENSP00000309757.6:n.1427+552T=
NM_000237.2:c.1427+552T= NP_000228.1:n.1427+552T=
NM_000237.3:c.1427+552T= MANE Select NP_000228.1:n.1427+552T=