Canonical Allele Identifier: CA2579105845
Gene: LPL HGNC NCBI

Linked Data

gnomAD v4: 8-19954064-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954064A>C , CM000670.2:g.19954064A>C GRCh38
NC_000008.10:g.19811575A>C , CM000670.1:g.19811575A>C GRCh37
NC_000008.9:g.19855855A>C NCBI36
NG_008855.1:g.19994A>C
NG_008855.2:g.57348A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.542-56A>C MANE Select ENSP00000497642.1:n.542-56A>C
ENST00000311322.8:c.542-56A>C ENSP00000309757.6:n.542-56A>C
ENST00000520959.5:c.314-56A>C ENSP00000428496.1:n.314-56A>C
NM_000237.2:c.542-56A>C NP_000228.1:n.542-56A>C
NM_000237.3:c.542-56A>C MANE Select NP_000228.1:n.542-56A>C