Canonical Allele Identifier: CA1769102051
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954187A= , CM000670.2:g.19954187A= GRCh38
NC_000008.10:g.19811698A= , CM000670.1:g.19811698A= GRCh37
NC_000008.9:g.19855978A= NCBI36
NG_008855.1:g.20117A=
NG_008855.2:g.57471A=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.609A= MANE Select ENSP00000497642.1:p.Ala203=
ENST00000311322.8:c.609A= ENSP00000309757.6:p.Ala203=
NM_000237.2:c.609A= NP_000228.1:p.Ala203=
NM_000237.3:c.609A= MANE Select NP_000228.1:p.Ala203=