Canonical Allele Identifier: CA370467018
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19805815C>A (hg19) chr8:g.19948304C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19948304C>A , CM000670.2:g.19948304C>A GRCh38
NC_000008.10:g.19805815C>A , CM000670.1:g.19805815C>A GRCh37
NC_000008.9:g.19850095C>A NCBI36
NG_008855.1:g.14234C>A
NG_008855.2:g.51588C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.213C>A MANE Select ENSP00000497642.1:p.His71Gln
ENST00000311322.8:c.213C>A ENSP00000309757.6:p.His71Gln
ENST00000520959.5:c.-16C>A ENSP00000428496.1:n.-16C>A
ENST00000521994.1:n.398C>A
ENST00000522701.5:c.213C>A ENSP00000428557.1:p.His71Gln
ENST00000523696.1:n.282C>A
ENST00000524029.5:c.213C>A ENSP00000428237.1:p.His71Gln
NM_000237.2:c.213C>A NP_000228.1:p.His71Gln
NM_000237.3:c.213C>A MANE Select NP_000228.1:p.His71Gln
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