Canonical Allele Identifier: CA1769101914
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954142_19954144delinsCTT , CM000670.2:g.19954142_19954144delinsCTT GRCh38
NC_000008.10:g.19811653_19811655delinsCTT , CM000670.1:g.19811653_19811655delinsCTT GRCh37
NC_000008.9:g.19855933_19855935delinsCTT NCBI36
NG_008855.1:g.20072_20074delinsCTT
NG_008855.2:g.57426_57428delinsCTT

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.564_566delinsCTT MANE Select ENSP00000497642.1:p.Asn188=
ENST00000311322.8:c.564_566delinsCTT ENSP00000309757.6:p.Asn188=
ENST00000520959.5:c.336_338delinsCTT ENSP00000428496.1:p.Asn112=
NM_000237.2:c.564_566delinsCTT NP_000228.1:p.Asn188=
NM_000237.3:c.564_566delinsCTT MANE Select NP_000228.1:p.Asn188=