Canonical Allele Identifier: CA370469179
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19813467T>A (hg19) chr8:g.19955956T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955956T>A , CM000670.2:g.19955956T>A GRCh38
NC_000008.10:g.19813467T>A , CM000670.1:g.19813467T>A GRCh37
NC_000008.9:g.19857747T>A NCBI36
NG_008855.1:g.21886T>A
NG_008855.2:g.59240T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.891T>A MANE Select ENSP00000497642.1:p.Phe297Leu
ENST00000311322.8:c.891T>A ENSP00000309757.6:p.Phe297Leu
NM_000237.2:c.891T>A NP_000228.1:p.Phe297Leu
NM_000237.3:c.891T>A MANE Select NP_000228.1:p.Phe297Leu
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