Canonical Allele Identifier: CA1769103109
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954508C= , CM000670.2:g.19954508C= GRCh38
NC_000008.10:g.19812019C= , CM000670.1:g.19812019C= GRCh37
NC_000008.9:g.19856299C= NCBI36
NG_008855.1:g.20438C=
NG_008855.2:g.57792C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.775+155C= MANE Select ENSP00000497642.1:n.775+155C=
ENST00000311322.8:c.775+155C= ENSP00000309757.6:n.775+155C=
NM_000237.2:c.775+155C= NP_000228.1:n.775+155C=
NM_000237.3:c.775+155C= MANE Select NP_000228.1:n.775+155C=