Canonical Allele Identifier: CA1769102542
Gene: LPL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954220A= , CM000670.2:g.19954220A= GRCh38
NC_000008.10:g.19811731A= , CM000670.1:g.19811731A= GRCh37
NC_000008.9:g.19856011A= NCBI36
NG_008855.1:g.20150A=
NG_008855.2:g.57504A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.642A= MANE Select ENSP00000497642.1:p.Arg214=
ENST00000311322.8:c.642A= ENSP00000309757.6:p.Arg214=
NM_000237.2:c.642A= NP_000228.1:p.Arg214=
NM_000237.3:c.642A= MANE Select NP_000228.1:p.Arg214=
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