Canonical Allele Identifier: CA580158086
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1200161229

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19957592_19957594del , CM000670.2:g.19957592_19957594del GRCh38
NC_000008.10:g.19815103_19815105del , CM000670.1:g.19815103_19815105del GRCh37
NC_000008.9:g.19859383_19859385del NCBI36
NG_008855.1:g.23522_23524del
NG_008855.2:g.60876_60878del

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1018+1509_1018+1511del MANE Select ENSP00000497642.1:n.1018+1509_1018+1511de...
ENST00000650478.1:c.79+1509_79+1511del ENSP00000497560.1:n.79+1509_79+1511del
ENST00000311322.8:c.1018+1509_1018+1511del ENSP00000309757.6:n.1018+1509_1018+1511de...
NM_000237.2:c.1018+1509_1018+1511del NP_000228.1:n.1018+1509_1018+1511del
NM_000237.3:c.1018+1509_1018+1511del MANE Select NP_000228.1:n.1018+1509_1018+1511del