Canonical Allele Identifier: CA2695208919
Gene: LPL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951831del , CM000670.2:g.19951831del GRCh38
NC_000008.10:g.19809342del , CM000670.1:g.19809342del GRCh37
NC_000008.9:g.19853622del NCBI36
NG_008855.1:g.17761del
NG_008855.2:g.55115del

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.312del MANE Select ENSP00000497642.1:p.Asp105ThrfsTer?
ENST00000311322.8:c.312del ENSP00000309757.6:p.Asp105ThrfsTer?
ENST00000520959.5:c.84del ENSP00000428496.1:p.Asp29ThrfsTer?
ENST00000522701.5:c.312del ENSP00000428557.1:p.Asp105ThrfsTer?
ENST00000524029.5:c.312del ENSP00000428237.1:p.Asp105ThrfsTer?
NM_000237.2:c.312del NP_000228.1:p.Asp105ThrfsTer?
NM_000237.3:c.312del MANE Select NP_000228.1:p.Asp105ThrfsTer?
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