Canonical Allele Identifier: CA1769101918
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954145T= , CM000670.2:g.19954145T= GRCh38
NC_000008.10:g.19811656T= , CM000670.1:g.19811656T= GRCh37
NC_000008.9:g.19855936T= NCBI36
NG_008855.1:g.20075T=
NG_008855.2:g.57429T=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.567T= MANE Select ENSP00000497642.1:p.Phe189=
ENST00000311322.8:c.567T= ENSP00000309757.6:p.Phe189=
ENST00000520959.5:c.339T= ENSP00000428496.1:p.Phe113=
NM_000237.2:c.567T= NP_000228.1:p.Phe189=
NM_000237.3:c.567T= MANE Select NP_000228.1:p.Phe189=