Canonical Allele Identifier: CA370468303
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954144T>A , CM000670.2:g.19954144T>A GRCh38
NC_000008.10:g.19811655T>A , CM000670.1:g.19811655T>A GRCh37
NC_000008.9:g.19855935T>A NCBI36
NG_008855.1:g.20074T>A
NG_008855.2:g.57428T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.566T>A MANE Select ENSP00000497642.1:p.Phe189Tyr
ENST00000311322.8:c.566T>A ENSP00000309757.6:p.Phe189Tyr
ENST00000520959.5:c.338T>A ENSP00000428496.1:p.Phe113Tyr
NM_000237.2:c.566T>A NP_000228.1:p.Phe189Tyr
NM_000237.3:c.566T>A MANE Select NP_000228.1:p.Phe189Tyr