Canonical Allele Identifier: CA370638567
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19818434A>G (hg19) chr8:g.19960923A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19960923A>G , CM000670.2:g.19960923A>G GRCh38
NC_000008.10:g.19818434A>G , CM000670.1:g.19818434A>G GRCh37
NC_000008.9:g.19862714A>G NCBI36
NG_008855.1:g.26853A>G
NG_008855.2:g.64207A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1162A>G MANE Select ENSP00000497642.1:p.Thr388Ala
ENST00000650478.1:c.102A>G ENSP00000497560.1:p.Arg34=
ENST00000311322.8:c.1162A>G ENSP00000309757.6:p.Thr388Ala
NM_000237.2:c.1162A>G NP_000228.1:p.Thr388Ala
NM_000237.3:c.1162A>G MANE Select NP_000228.1:p.Thr388Ala
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Search 100 bp 3'