Canonical Allele Identifier: CA2686364583
Gene: LPL HGNC NCBI

Linked Data

gnomAD v4: 8-19966843-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19966843G>T , CM000670.2:g.19966843G>T GRCh38
NC_000008.10:g.19824354G>T , CM000670.1:g.19824354G>T GRCh37
NC_000008.9:g.19868634G>T NCBI36
NG_008855.1:g.32773G>T
NG_008855.2:g.70127G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.*1533G>T MANE Select ENSP00000497642.1:n.*1533G>T
ENST00000650478.1:c.1901G>T ENSP00000497560.1:n.1901G>T
ENST00000311322.8:c.*1533G>T ENSP00000309757.6:n.*1533G>T
NM_000237.2:c.*1533G>T NP_000228.1:n.*1533G>T
NM_000237.3:c.*1533G>T MANE Select NP_000228.1:n.*1533G>T