Canonical Allele Identifier: CA370468292
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954140A>C , CM000670.2:g.19954140A>C GRCh38
NC_000008.10:g.19811651A>C , CM000670.1:g.19811651A>C GRCh37
NC_000008.9:g.19855931A>C NCBI36
NG_008855.1:g.20070A>C
NG_008855.2:g.57424A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.562A>C MANE Select ENSP00000497642.1:p.Asn188His
ENST00000311322.8:c.562A>C ENSP00000309757.6:p.Asn188His
ENST00000520959.5:c.334A>C ENSP00000428496.1:p.Asn112His
NM_000237.2:c.562A>C NP_000228.1:p.Asn188His
NM_000237.3:c.562A>C MANE Select NP_000228.1:p.Asn188His