Canonical Allele Identifier: CA1111553129
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs2069997264
gnomAD v3: 8-19957544-G-A
gnomAD v4: 8-19957544-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19957544G>A , CM000670.2:g.19957544G>A GRCh38
NC_000008.10:g.19815055G>A , CM000670.1:g.19815055G>A GRCh37
NC_000008.9:g.19859335G>A NCBI36
NG_008855.1:g.23474G>A
NG_008855.2:g.60828G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1018+1461G>A MANE Select ENSP00000497642.1:n.1018+1461G>A
ENST00000650478.1:c.79+1461G>A ENSP00000497560.1:n.79+1461G>A
ENST00000311322.8:c.1018+1461G>A ENSP00000309757.6:n.1018+1461G>A
NM_000237.2:c.1018+1461G>A NP_000228.1:n.1018+1461G>A
NM_000237.3:c.1018+1461G>A MANE Select NP_000228.1:n.1018+1461G>A