Canonical Allele Identifier: CA370468304
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.566T>C MANE Select ENSP00000497642.1:p.Phe189Ser
ENST00000311322.8:c.566T>C ENSP00000309757.6:p.Phe189Ser
ENST00000520959.5:c.338T>C ENSP00000428496.1:p.Phe113Ser
NM_000237.2:c.566T>C NP_000228.1:p.Phe189Ser
NM_000237.3:c.566T>C MANE Select NP_000228.1:p.Phe189Ser