Canonical Allele Identifier: CA2779304343
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19962808A>C , CM000670.2:g.19962808A>C GRCh38
NC_000008.10:g.19820319A>C , CM000670.1:g.19820319A>C GRCh37
NC_000008.9:g.19864599A>C NCBI36
NG_008855.1:g.28738A>C
NG_008855.2:g.66092A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1427+589A>C MANE Select ENSP00000497642.1:n.1427+589A>C
ENST00000650478.1:c.367+589A>C ENSP00000497560.1:n.367+589A>C
ENST00000311322.8:c.1427+589A>C ENSP00000309757.6:n.1427+589A>C
NM_000237.2:c.1427+589A>C NP_000228.1:n.1427+589A>C
NM_000237.3:c.1427+589A>C MANE Select NP_000228.1:n.1427+589A>C