Canonical Allele Identifier: CA2779304284
Gene: LPL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954061_19954071dup , CM000670.2:g.19954061_19954071dup GRCh38
NC_000008.10:g.19811572_19811582dup , CM000670.1:g.19811572_19811582dup GRCh37
NC_000008.9:g.19855852_19855862dup NCBI36
NG_008855.1:g.19991_20001dup
NG_008855.2:g.57345_57355dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.542-59_542-49dup MANE Select ENSP00000497642.1:n.542-59_542-49dup
ENST00000311322.8:c.542-59_542-49dup ENSP00000309757.6:n.542-59_542-49dup
ENST00000520959.5:c.314-59_314-49dup ENSP00000428496.1:n.314-59_314-49dup
NM_000237.2:c.542-59_542-49dup NP_000228.1:n.542-59_542-49dup
NM_000237.3:c.542-59_542-49dup MANE Select NP_000228.1:n.542-59_542-49dup
Search 100 bp 5'
Search 100 bp 3'