Canonical Allele Identifier: CA370468302
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19811654T>A (hg19) chr8:g.19954143T>A (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.565T>A MANE Select ENSP00000497642.1:p.Phe189Ile
ENST00000311322.8:c.565T>A ENSP00000309757.6:p.Phe189Ile
ENST00000520959.5:c.337T>A ENSP00000428496.1:p.Phe113Ile
NM_000237.2:c.565T>A NP_000228.1:p.Phe189Ile
NM_000237.3:c.565T>A MANE Select NP_000228.1:p.Phe189Ile
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