Canonical Allele Identifier: CA1769104183
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955559C= , CM000670.2:g.19955559C= GRCh38
NC_000008.10:g.19813070C= , CM000670.1:g.19813070C= GRCh37
NC_000008.9:g.19857350C= NCBI36
NG_008855.1:g.21489C=
NG_008855.2:g.58843C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.776-282C= MANE Select ENSP00000497642.1:n.776-282C=
ENST00000311322.8:c.776-282C= ENSP00000309757.6:n.776-282C=
NM_000237.2:c.776-282C= NP_000228.1:n.776-282C=
NM_000237.3:c.776-282C= MANE Select NP_000228.1:n.776-282C=