Canonical Allele Identifier: CA370638566
Gene: LPL HGNC NCBI

Linked Data

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

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

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1162A>C MANE Select ENSP00000497642.1:p.Thr388Pro
ENST00000650478.1:c.102A>C ENSP00000497560.1:p.Arg34Ser
ENST00000311322.8:c.1162A>C ENSP00000309757.6:p.Thr388Pro
NM_000237.2:c.1162A>C NP_000228.1:p.Thr388Pro
NM_000237.3:c.1162A>C MANE Select NP_000228.1:p.Thr388Pro
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