Canonical Allele Identifier: CA1769103963
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955333C= , CM000670.2:g.19955333C= GRCh38
NC_000008.10:g.19812844C= , CM000670.1:g.19812844C= GRCh37
NC_000008.9:g.19857124C= NCBI36
NG_008855.1:g.21263C=
NG_008855.2:g.58617C=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.776-508C= MANE Select ENSP00000497642.1:n.776-508C=
ENST00000311322.8:c.776-508C= ENSP00000309757.6:n.776-508C=
NM_000237.2:c.776-508C= NP_000228.1:n.776-508C=
NM_000237.3:c.776-508C= MANE Select NP_000228.1:n.776-508C=