Canonical Allele Identifier: CA2686357408
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939366_19939375del , CM000670.2:g.19939366_19939375del GRCh38
NC_000008.10:g.19796877_19796886del , CM000670.1:g.19796877_19796886del GRCh37
NC_000008.9:g.19841157_19841166del NCBI36
NG_008855.1:g.5296_5305del
NG_008855.2:g.42650_42659del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.-75_-66del MANE Select ENSP00000497642.1:n.-75_-66del
ENST00000311322.8:c.-75_-66del ENSP00000309757.6:n.-75_-66del
ENST00000519773.1:c.-75_-66del ENSP00000431028.1:n.-75_-66del
ENST00000520959.5:c.-140-8814_-140-8805del ENSP00000428496.1:n.-140-8814_-140-8805del
ENST00000521994.1:n.111_120del
ENST00000522701.5:c.-75_-66del ENSP00000428557.1:n.-75_-66del
ENST00000524029.5:c.-75_-66del ENSP00000428237.1:n.-75_-66del
NM_000237.2:c.-75_-66del NP_000228.1:n.-75_-66del
NM_000237.3:c.-75_-66del MANE Select NP_000228.1:n.-75_-66del