Canonical Allele Identifier: CA1769083374
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1304688882
gnomAD v4: 8-19939383-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939383C>T , CM000670.2:g.19939383C>T GRCh38
NC_000008.10:g.19796894C>T , CM000670.1:g.19796894C>T GRCh37
NC_000008.9:g.19841174C>T NCBI36
NG_008855.1:g.5313C>T
NG_008855.2:g.42667C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.-58C>T MANE Select ENSP00000497642.1:n.-58C>T
ENST00000311322.8:c.-58C>T ENSP00000309757.6:n.-58C>T
ENST00000519773.1:c.-58C>T ENSP00000431028.1:n.-58C>T
ENST00000520959.5:c.-140-8797C>T ENSP00000428496.1:n.-140-8797C>T
ENST00000521994.1:n.128C>T
ENST00000522701.5:c.-58C>T ENSP00000428557.1:n.-58C>T
ENST00000523696.1:n.12C>T
ENST00000524029.5:c.-58C>T ENSP00000428237.1:n.-58C>T
NM_000237.2:c.-58C>T NP_000228.1:n.-58C>T
NM_000237.3:c.-58C>T MANE Select NP_000228.1:n.-58C>T