Canonical Allele Identifier: CA2686364534
Gene: LPL HGNC NCBI

Linked Data

gnomAD v4: 8-19966639-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19966639G>T , CM000670.2:g.19966639G>T GRCh38
NC_000008.10:g.19824150G>T , CM000670.1:g.19824150G>T GRCh37
NC_000008.9:g.19868430G>T NCBI36
NG_008855.1:g.32569G>T
NG_008855.2:g.69923G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.*1329G>T MANE Select ENSP00000497642.1:n.*1329G>T
ENST00000650478.1:c.1697G>T ENSP00000497560.1:n.1697G>T
ENST00000311322.8:c.*1329G>T ENSP00000309757.6:n.*1329G>T
NM_000237.2:c.*1329G>T NP_000228.1:n.*1329G>T
NM_000237.3:c.*1329G>T MANE Select NP_000228.1:n.*1329G>T
Search 100 bp 5'
Search 100 bp 3'