Canonical Allele Identifier: CA1111556516
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19961712_19961713dup , CM000670.2:g.19961712_19961713dup GRCh38
NC_000008.10:g.19819223_19819224dup , CM000670.1:g.19819223_19819224dup GRCh37
NC_000008.9:g.19863503_19863504dup NCBI36
NG_008855.1:g.27642_27643dup
NG_008855.2:g.64996_64997dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1323-403_1323-402dup MANE Select ENSP00000497642.1:n.1323-403_1323-402dup
ENST00000650478.1:c.263-403_263-402dup ENSP00000497560.1:n.263-403_263-402dup
ENST00000311322.8:c.1323-403_1323-402dup ENSP00000309757.6:n.1323-403_1323-402dup
NM_000237.2:c.1323-403_1323-402dup NP_000228.1:n.1323-403_1323-402dup
NM_000237.3:c.1323-403_1323-402dup MANE Select NP_000228.1:n.1323-403_1323-402dup