Canonical Allele Identifier: CA370468288
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19811648C>A (hg19) chr8:g.19954137C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954137C>A , CM000670.2:g.19954137C>A GRCh38
NC_000008.10:g.19811648C>A , CM000670.1:g.19811648C>A GRCh37
NC_000008.9:g.19855928C>A NCBI36
NG_008855.1:g.20067C>A
NG_008855.2:g.57421C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.559C>A MANE Select ENSP00000497642.1:p.Pro187Thr
ENST00000311322.8:c.559C>A ENSP00000309757.6:p.Pro187Thr
ENST00000520959.5:c.331C>A ENSP00000428496.1:p.Pro111Thr
NM_000237.2:c.559C>A NP_000228.1:p.Pro187Thr
NM_000237.3:c.559C>A MANE Select NP_000228.1:p.Pro187Thr
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