Canonical Allele Identifier: CA849561570
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1222729241

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19957808T>C , CM000670.2:g.19957808T>C GRCh38
NC_000008.10:g.19815319T>C , CM000670.1:g.19815319T>C GRCh37
NC_000008.9:g.19859599T>C NCBI36
NG_008855.1:g.23738T>C
NG_008855.2:g.61092T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1019-1452T>C MANE Select ENSP00000497642.1:n.1019-1452T>C
ENST00000650478.1:c.79+1725T>C ENSP00000497560.1:n.79+1725T>C
ENST00000311322.8:c.1019-1452T>C ENSP00000309757.6:n.1019-1452T>C
NM_000237.2:c.1019-1452T>C NP_000228.1:n.1019-1452T>C
NM_000237.3:c.1019-1452T>C MANE Select NP_000228.1:n.1019-1452T>C