Canonical Allele Identifier: CA370468301
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954143T>G , CM000670.2:g.19954143T>G GRCh38
NC_000008.10:g.19811654T>G , CM000670.1:g.19811654T>G GRCh37
NC_000008.9:g.19855934T>G NCBI36
NG_008855.1:g.20073T>G
NG_008855.2:g.57427T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.565T>G MANE Select ENSP00000497642.1:p.Phe189Val
ENST00000311322.8:c.565T>G ENSP00000309757.6:p.Phe189Val
ENST00000520959.5:c.337T>G ENSP00000428496.1:p.Phe113Val
NM_000237.2:c.565T>G NP_000228.1:p.Phe189Val
NM_000237.3:c.565T>G MANE Select NP_000228.1:p.Phe189Val