Canonical Allele Identifier: CA1769108051
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19958817C= , CM000670.2:g.19958817C= GRCh38
NC_000008.10:g.19816328C= , CM000670.1:g.19816328C= GRCh37
NC_000008.9:g.19860608C= NCBI36
NG_008855.1:g.24747C=
NG_008855.2:g.62101C=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1019-443C= MANE Select ENSP00000497642.1:n.1019-443C=
ENST00000650478.1:c.80-2084C= ENSP00000497560.1:n.80-2084C=
ENST00000311322.8:c.1019-443C= ENSP00000309757.6:n.1019-443C=
NM_000237.2:c.1019-443C= NP_000228.1:n.1019-443C=
NM_000237.3:c.1019-443C= MANE Select NP_000228.1:n.1019-443C=