Canonical Allele Identifier: CA2686357389
Gene: LPL HGNC NCBI

Linked Data

gnomAD v4: 8-19939342-C-CTTT
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939342_19939343insTTT , CM000670.2:g.19939342_19939343insTTT GRCh38
NC_000008.10:g.19796853_19796854insTTT , CM000670.1:g.19796853_19796854insTTT GRCh37
NC_000008.9:g.19841133_19841134insTTT NCBI36
NG_008855.1:g.5272_5273insTTT
NG_008855.2:g.42626_42627insTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.-99_-98insTTT MANE Select ENSP00000497642.1:n.-99_-98insTTT
ENST00000311322.8:c.-99_-98insTTT ENSP00000309757.6:n.-99_-98insTTT
ENST00000519773.1:c.-99_-98insTTT ENSP00000431028.1:n.-99_-98insTTT
ENST00000520959.5:c.-140-8838_-140-8837insTTT ENSP00000428496.1:n.-140-8838_-140-8837insTTT
ENST00000521994.1:n.87_88insTTT
ENST00000522701.5:c.-99_-98insTTT ENSP00000428557.1:n.-99_-98insTTT
ENST00000524029.5:c.-99_-98insTTT ENSP00000428237.1:n.-99_-98insTTT
NM_000237.2:c.-99_-98insTTT NP_000228.1:n.-99_-98insTTT
NM_000237.3:c.-99_-98insTTT MANE Select NP_000228.1:n.-99_-98insTTT
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