Canonical Allele Identifier: CA370467741
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951932T>C , CM000670.2:g.19951932T>C GRCh38
NC_000008.10:g.19809443T>C , CM000670.1:g.19809443T>C GRCh37
NC_000008.9:g.19853723T>C NCBI36
NG_008855.1:g.17862T>C
NG_008855.2:g.55216T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.413T>C MANE Select ENSP00000497642.1:p.Phe138Ser
ENST00000311322.8:c.413T>C ENSP00000309757.6:p.Phe138Ser
ENST00000520959.5:c.185T>C ENSP00000428496.1:p.Phe62Ser
NM_000237.2:c.413T>C NP_000228.1:p.Phe138Ser
NM_000237.3:c.413T>C MANE Select NP_000228.1:p.Phe138Ser