Canonical Allele Identifier: CA370468299
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954142C>G , CM000670.2:g.19954142C>G GRCh38
NC_000008.10:g.19811653C>G , CM000670.1:g.19811653C>G GRCh37
NC_000008.9:g.19855933C>G NCBI36
NG_008855.1:g.20072C>G
NG_008855.2:g.57426C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.564C>G MANE Select ENSP00000497642.1:p.Asn188Lys
ENST00000311322.8:c.564C>G ENSP00000309757.6:p.Asn188Lys
ENST00000520959.5:c.336C>G ENSP00000428496.1:p.Asn112Lys
NM_000237.2:c.564C>G NP_000228.1:p.Asn188Lys
NM_000237.3:c.564C>G MANE Select NP_000228.1:p.Asn188Lys