Canonical Allele Identifier: CA2686357349
Gene: LPL HGNC NCBI

Linked Data

gnomAD v4: 8-19939305-TA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939306del , CM000670.2:g.19939306del GRCh38
NC_000008.10:g.19796817del , CM000670.1:g.19796817del GRCh37
NC_000008.9:g.19841097del NCBI36
NG_008855.1:g.5236del
NG_008855.2:g.42590del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.-135del MANE Select ENSP00000497642.1:n.-135del
ENST00000311322.8:c.-135del ENSP00000309757.6:n.-135del
ENST00000519773.1:c.-135del ENSP00000431028.1:n.-135del
ENST00000520959.5:c.-140-8874del ENSP00000428496.1:n.-140-8874del
ENST00000521994.1:n.51del
ENST00000522701.5:c.-135del ENSP00000428557.1:n.-135del
ENST00000524029.5:c.-135del ENSP00000428237.1:n.-135del
NM_000237.2:c.-135del NP_000228.1:n.-135del
NM_000237.3:c.-135del MANE Select NP_000228.1:n.-135del
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