Canonical Allele Identifier: CA370467548
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951838A>T , CM000670.2:g.19951838A>T GRCh38
NC_000008.10:g.19809349A>T , CM000670.1:g.19809349A>T GRCh37
NC_000008.9:g.19853629A>T NCBI36
NG_008855.1:g.17768A>T
NG_008855.2:g.55122A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.319A>T MANE Select ENSP00000497642.1:p.Asn107Tyr
ENST00000311322.8:c.319A>T ENSP00000309757.6:p.Asn107Tyr
ENST00000520959.5:c.91A>T ENSP00000428496.1:p.Asn31Tyr
ENST00000524029.5:c.319A>T ENSP00000428237.1:p.Asn107Tyr
NM_000237.2:c.319A>T NP_000228.1:p.Asn107Tyr
NM_000237.3:c.319A>T MANE Select NP_000228.1:p.Asn107Tyr