Canonical Allele Identifier: CA459879555
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19811860T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954349T>A , CM000670.2:g.19954349T>A GRCh38
NC_000008.10:g.19811860T>A , CM000670.1:g.19811860T>A GRCh37
NC_000008.9:g.19856140T>A NCBI36
NG_008855.1:g.20279T>A
NG_008855.2:g.57633T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.771T>A MANE Select ENSP00000497642.1:p.Leu257=
ENST00000311322.8:c.771T>A ENSP00000309757.6:p.Leu257=
NM_000237.2:c.771T>A NP_000228.1:p.Leu257=
NM_000237.3:c.771T>A MANE Select NP_000228.1:p.Leu257=
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