Canonical Allele Identifier: CA1769097113
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs987581938
gnomAD v4: 8-19951571-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951571C>A , CM000670.2:g.19951571C>A GRCh38
NC_000008.10:g.19809082C>A , CM000670.1:g.19809082C>A GRCh37
NC_000008.9:g.19853362C>A NCBI36
NG_008855.1:g.17501C>A
NG_008855.2:g.54855C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.250-198C>A MANE Select ENSP00000497642.1:n.250-198C>A
ENST00000311322.8:c.250-198C>A ENSP00000309757.6:n.250-198C>A
ENST00000520959.5:c.22-198C>A ENSP00000428496.1:n.22-198C>A
ENST00000521994.1:n.435-126C>A
ENST00000522701.5:c.250-198C>A ENSP00000428557.1:n.250-198C>A
ENST00000524029.5:c.250-198C>A ENSP00000428237.1:n.250-198C>A
NM_000237.2:c.250-198C>A NP_000228.1:n.250-198C>A
NM_000237.3:c.250-198C>A MANE Select NP_000228.1:n.250-198C>A