Canonical Allele Identifier: CA1769102694
Gene: LPL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954265T= , CM000670.2:g.19954265T= GRCh38
NC_000008.10:g.19811776T= , CM000670.1:g.19811776T= GRCh37
NC_000008.9:g.19856056T= NCBI36
NG_008855.1:g.20195T=
NG_008855.2:g.57549T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.687T= MANE Select ENSP00000497642.1:p.His229=
ENST00000311322.8:c.687T= ENSP00000309757.6:p.His229=
NM_000237.2:c.687T= NP_000228.1:p.His229=
NM_000237.3:c.687T= MANE Select NP_000228.1:p.His229=
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