Canonical Allele Identifier: CA370468586
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954281A>G , CM000670.2:g.19954281A>G GRCh38
NC_000008.10:g.19811792A>G , CM000670.1:g.19811792A>G GRCh37
NC_000008.9:g.19856072A>G NCBI36
NG_008855.1:g.20211A>G
NG_008855.2:g.57565A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.703A>G MANE Select ENSP00000497642.1:p.Asn235Asp
ENST00000311322.8:c.703A>G ENSP00000309757.6:p.Asn235Asp
NM_000237.2:c.703A>G NP_000228.1:p.Asn235Asp
NM_000237.3:c.703A>G MANE Select NP_000228.1:p.Asn235Asp