Canonical Allele Identifier: CA849561411
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1398156592

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19957491dup , CM000670.2:g.19957491dup GRCh38
NC_000008.10:g.19815002dup , CM000670.1:g.19815002dup GRCh37
NC_000008.9:g.19859282dup NCBI36
NG_008855.1:g.23421dup
NG_008855.2:g.60775dup

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1018+1408dup MANE Select ENSP00000497642.1:n.1018+1408dup
ENST00000650478.1:c.79+1408dup ENSP00000497560.1:n.79+1408dup
ENST00000311322.8:c.1018+1408dup ENSP00000309757.6:n.1018+1408dup
NM_000237.2:c.1018+1408dup NP_000228.1:n.1018+1408dup
NM_000237.3:c.1018+1408dup MANE Select NP_000228.1:n.1018+1408dup