Canonical Allele Identifier: CA1769102642
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954250G= , CM000670.2:g.19954250G= GRCh38
NC_000008.10:g.19811761G= , CM000670.1:g.19811761G= GRCh37
NC_000008.9:g.19856041G= NCBI36
NG_008855.1:g.20180G=
NG_008855.2:g.57534G=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.672G= MANE Select ENSP00000497642.1:p.Gln224=
ENST00000311322.8:c.672G= ENSP00000309757.6:p.Gln224=
NM_000237.2:c.672G= NP_000228.1:p.Gln224=
NM_000237.3:c.672G= MANE Select NP_000228.1:p.Gln224=