Canonical Allele Identifier: CA1769116338
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19966623C= , CM000670.2:g.19966623C= GRCh38
NC_000008.10:g.19824134C= , CM000670.1:g.19824134C= GRCh37
NC_000008.9:g.19868414C= NCBI36
NG_008855.1:g.32553C=
NG_008855.2:g.69907C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.*1313C= MANE Select ENSP00000497642.1:n.*1313C=
ENST00000650478.1:c.1681C= ENSP00000497560.1:n.1681C=
ENST00000311322.8:c.*1313C= ENSP00000309757.6:n.*1313C=
NM_000237.2:c.*1313C= NP_000228.1:n.*1313C=
NM_000237.3:c.*1313C= MANE Select NP_000228.1:n.*1313C=