Canonical Allele Identifier: CA2579105711
Gene: LPL HGNC NCBI

Linked Data

gnomAD v4: 8-19939393-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19939393A>G , CM000670.2:g.19939393A>G GRCh38
NC_000008.10:g.19796904A>G , CM000670.1:g.19796904A>G GRCh37
NC_000008.9:g.19841184A>G NCBI36
NG_008855.1:g.5323A>G
NG_008855.2:g.42677A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.-48A>G MANE Select ENSP00000497642.1:n.-48A>G
ENST00000311322.8:c.-48A>G ENSP00000309757.6:n.-48A>G
ENST00000519773.1:c.-48A>G ENSP00000431028.1:n.-48A>G
ENST00000520959.5:c.-140-8787A>G ENSP00000428496.1:n.-140-8787A>G
ENST00000521994.1:n.138A>G
ENST00000522701.5:c.-48A>G ENSP00000428557.1:n.-48A>G
ENST00000523696.1:n.22A>G
ENST00000524029.5:c.-48A>G ENSP00000428237.1:n.-48A>G
NM_000237.2:c.-48A>G NP_000228.1:n.-48A>G
NM_000237.3:c.-48A>G MANE Select NP_000228.1:n.-48A>G