Canonical Allele Identifier: CA2686360441
Gene: LPL HGNC NCBI

Linked Data

gnomAD v4: 8-19954103-CT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954109del , CM000670.2:g.19954109del GRCh38
NC_000008.10:g.19811620del , CM000670.1:g.19811620del GRCh37
NC_000008.9:g.19855900del NCBI36
NG_008855.1:g.20039del
NG_008855.2:g.57393del

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.542-11del MANE Select ENSP00000497642.1:n.542-11del
ENST00000311322.8:c.542-11del ENSP00000309757.6:n.542-11del
ENST00000520959.5:c.314-11del ENSP00000428496.1:n.314-11del
NM_000237.2:c.542-11del NP_000228.1:n.542-11del
NM_000237.3:c.542-11del MANE Select NP_000228.1:n.542-11del
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Search 100 bp 3'