Canonical Allele Identifier: CA1769104284
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955660G= , CM000670.2:g.19955660G= GRCh38
NC_000008.10:g.19813171G= , CM000670.1:g.19813171G= GRCh37
NC_000008.9:g.19857451G= NCBI36
NG_008855.1:g.21590G=
NG_008855.2:g.58944G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.776-181G= MANE Select ENSP00000497642.1:n.776-181G=
ENST00000311322.8:c.776-181G= ENSP00000309757.6:n.776-181G=
NM_000237.2:c.776-181G= NP_000228.1:n.776-181G=
NM_000237.3:c.776-181G= MANE Select NP_000228.1:n.776-181G=