Canonical Allele Identifier: CA1769097692
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951837C= , CM000670.2:g.19951837C= GRCh38
NC_000008.10:g.19809348C= , CM000670.1:g.19809348C= GRCh37
NC_000008.9:g.19853628C= NCBI36
NG_008855.1:g.17767C=
NG_008855.2:g.55121C=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.318C= MANE Select ENSP00000497642.1:p.Ser106=
ENST00000311322.8:c.318C= ENSP00000309757.6:p.Ser106=
ENST00000520959.5:c.90C= ENSP00000428496.1:p.Ser30=
ENST00000524029.5:c.318C= ENSP00000428237.1:p.Ser106=
NM_000237.2:c.318C= NP_000228.1:p.Ser106=
NM_000237.3:c.318C= MANE Select NP_000228.1:p.Ser106=