Canonical Allele Identifier: CA1769101910
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954137C= , CM000670.2:g.19954137C= GRCh38
NC_000008.10:g.19811648C= , CM000670.1:g.19811648C= GRCh37
NC_000008.9:g.19855928C= NCBI36
NG_008855.1:g.20067C=
NG_008855.2:g.57421C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.559C= MANE Select ENSP00000497642.1:p.Pro187=
ENST00000311322.8:c.559C= ENSP00000309757.6:p.Pro187=
ENST00000520959.5:c.331C= ENSP00000428496.1:p.Pro111=
NM_000237.2:c.559C= NP_000228.1:p.Pro187=
NM_000237.3:c.559C= MANE Select NP_000228.1:p.Pro187=