Canonical Allele Identifier: CA370467770
Gene: LPL HGNC NCBI

Linked Data

gnomAD v4: 8-19951943-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951943A>G , CM000670.2:g.19951943A>G GRCh38
NC_000008.10:g.19809454A>G , CM000670.1:g.19809454A>G GRCh37
NC_000008.9:g.19853734A>G NCBI36
NG_008855.1:g.17873A>G
NG_008855.2:g.55227A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.424A>G MANE Select ENSP00000497642.1:p.Met142Val
ENST00000311322.8:c.424A>G ENSP00000309757.6:p.Met142Val
ENST00000520959.5:c.196A>G ENSP00000428496.1:p.Met66Val
NM_000237.2:c.424A>G NP_000228.1:p.Met142Val
NM_000237.3:c.424A>G MANE Select NP_000228.1:p.Met142Val