Canonical Allele Identifier: CA918215200
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1563574904

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954098dup , CM000670.2:g.19954098dup GRCh38
NC_000008.10:g.19811609dup , CM000670.1:g.19811609dup GRCh37
NC_000008.9:g.19855889dup NCBI36
NG_008855.1:g.20028dup
NG_008855.2:g.57382dup

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.542-22dup MANE Select ENSP00000497642.1:n.542-22dup
ENST00000311322.8:c.542-22dup ENSP00000309757.6:n.542-22dup
ENST00000520959.5:c.314-22dup ENSP00000428496.1:n.314-22dup
NM_000237.2:c.542-22dup NP_000228.1:n.542-22dup
NM_000237.3:c.542-22dup MANE Select NP_000228.1:n.542-22dup