Canonical Allele Identifier: CA2686360536
Gene: LPL HGNC NCBI

Linked Data

gnomAD v4: 8-19955689-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955689C>T , CM000670.2:g.19955689C>T GRCh38
NC_000008.10:g.19813200C>T , CM000670.1:g.19813200C>T GRCh37
NC_000008.9:g.19857480C>T NCBI36
NG_008855.1:g.21619C>T
NG_008855.2:g.58973C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.776-152C>T MANE Select ENSP00000497642.1:n.776-152C>T
ENST00000311322.8:c.776-152C>T ENSP00000309757.6:n.776-152C>T
NM_000237.2:c.776-152C>T NP_000228.1:n.776-152C>T
NM_000237.3:c.776-152C>T MANE Select NP_000228.1:n.776-152C>T