Canonical Allele Identifier: CA12903534
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs331

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19962894G>A , CM000670.2:g.19962894G>A GRCh38
NC_000008.10:g.19820405G>A , CM000670.1:g.19820405G>A GRCh37
NC_000008.9:g.19864685G>A NCBI36
NG_008855.1:g.28824G>A
NG_008855.2:g.66178G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1427+675G>A MANE Select ENSP00000497642.1:p.=
ENST00000650478.1:n.367+675G>A ENSP00000497560.1:p.=
ENST00000311322.8:c.1427+675G>A ENSP00000309757.6:p.=
NM_000237.2:c.1427+675G>A NP_000228.1:p.=
NM_000237.3:c.1427+675G>A MANE Select NP_000228.1:p.=