Canonical Allele Identifier: CA370467537
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951833A>T , CM000670.2:g.19951833A>T GRCh38
NC_000008.10:g.19809344A>T , CM000670.1:g.19809344A>T GRCh37
NC_000008.9:g.19853624A>T NCBI36
NG_008855.1:g.17763A>T
NG_008855.2:g.55117A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.314A>T MANE Select ENSP00000497642.1:p.Asp105Val
ENST00000311322.8:c.314A>T ENSP00000309757.6:p.Asp105Val
ENST00000520959.5:c.86A>T ENSP00000428496.1:p.Asp29Val
ENST00000522701.5:c.314A>T ENSP00000428557.1:p.Asp105Val
ENST00000524029.5:c.314A>T ENSP00000428237.1:p.Asp105Val
NM_000237.2:c.314A>T NP_000228.1:p.Asp105Val
NM_000237.3:c.314A>T MANE Select NP_000228.1:p.Asp105Val