Canonical Allele Identifier: CA1769102713
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954271C= , CM000670.2:g.19954271C= GRCh38
NC_000008.10:g.19811782C= , CM000670.1:g.19811782C= GRCh37
NC_000008.9:g.19856062C= NCBI36
NG_008855.1:g.20201C=
NG_008855.2:g.57555C=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.693C= MANE Select ENSP00000497642.1:p.Asp231=
ENST00000311322.8:c.693C= ENSP00000309757.6:p.Asp231=
NM_000237.2:c.693C= NP_000228.1:p.Asp231=
NM_000237.3:c.693C= MANE Select NP_000228.1:p.Asp231=