Canonical Allele Identifier: CA2695199656
Gene: LPL HGNC NCBI

Linked Data

ClinVar Variation Id: 1521
ClinVar RCV Id: RCV000001585

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955963_19958026dup , CM000670.2:g.19955963_19958026dup GRCh38
NC_000008.10:g.19813474_19815537dup , CM000670.1:g.19813474_19815537dup GRCh37
NC_000008.9:g.19857754_19859817dup NCBI36
NG_008855.1:g.21893_23956dup
NG_008855.2:g.59247_61310dup

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.898_1019-1234dup
ENST00000311322.8:c.898_1019-1234dup
NM_000237.2:c.898_1019-1234dup
NM_000237.3:c.898_1019-1234dup