Canonical Allele Identifier: CA459719163
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19818460G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19960949G>A , CM000670.2:g.19960949G>A GRCh38
NC_000008.10:g.19818460G>A , CM000670.1:g.19818460G>A GRCh37
NC_000008.9:g.19862740G>A NCBI36
NG_008855.1:g.26879G>A
NG_008855.2:g.64233G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1188G>A MANE Select ENSP00000497642.1:p.Glu396=
ENST00000650478.1:c.128G>A ENSP00000497560.1:n.128G>A
ENST00000311322.8:c.1188G>A ENSP00000309757.6:p.Glu396=
NM_000237.2:c.1188G>A NP_000228.1:p.Glu396=
NM_000237.3:c.1188G>A MANE Select NP_000228.1:p.Glu396=
Search 100 bp 5'
Search 100 bp 3'