Canonical Allele Identifier: CA2779304283
Gene: LPL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954048T>C , CM000670.2:g.19954048T>C GRCh38
NC_000008.10:g.19811559T>C , CM000670.1:g.19811559T>C GRCh37
NC_000008.9:g.19855839T>C NCBI36
NG_008855.1:g.19978T>C
NG_008855.2:g.57332T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.542-72T>C MANE Select ENSP00000497642.1:n.542-72T>C
ENST00000311322.8:c.542-72T>C ENSP00000309757.6:n.542-72T>C
ENST00000520959.5:c.314-72T>C ENSP00000428496.1:n.314-72T>C
NM_000237.2:c.542-72T>C NP_000228.1:n.542-72T>C
NM_000237.3:c.542-72T>C MANE Select NP_000228.1:n.542-72T>C
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