Canonical Allele Identifier: CA1769102819
Gene: LPL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954322T= , CM000670.2:g.19954322T= GRCh38
NC_000008.10:g.19811833T= , CM000670.1:g.19811833T= GRCh37
NC_000008.9:g.19856113T= NCBI36
NG_008855.1:g.20252T=
NG_008855.2:g.57606T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.744T= MANE Select ENSP00000497642.1:p.Ala248=
ENST00000311322.8:c.744T= ENSP00000309757.6:p.Ala248=
NM_000237.2:c.744T= NP_000228.1:p.Ala248=
NM_000237.3:c.744T= MANE Select NP_000228.1:p.Ala248=
Search 100 bp 5'
Search 100 bp 3'