Canonical Allele Identifier: CA173378935
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs547434548

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19957559A>G , CM000670.2:g.19957559A>G GRCh38
NC_000008.10:g.19815070A>G , CM000670.1:g.19815070A>G GRCh37
NC_000008.9:g.19859350A>G NCBI36
NG_008855.1:g.23489A>G
NG_008855.2:g.60843A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1018+1476A>G MANE Select ENSP00000497642.1:p.=
ENST00000650478.1:n.79+1476A>G ENSP00000497560.1:p.=
ENST00000311322.8:c.1018+1476A>G ENSP00000309757.6:p.=
NM_000237.2:c.1018+1476A>G NP_000228.1:p.=
NM_000237.3:c.1018+1476A>G MANE Select NP_000228.1:p.=