Canonical Allele Identifier: CA370467535
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951832G>T , CM000670.2:g.19951832G>T GRCh38
NC_000008.10:g.19809343G>T , CM000670.1:g.19809343G>T GRCh37
NC_000008.9:g.19853623G>T NCBI36
NG_008855.1:g.17762G>T
NG_008855.2:g.55116G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.313G>T MANE Select ENSP00000497642.1:p.Asp105Tyr
ENST00000311322.8:c.313G>T ENSP00000309757.6:p.Asp105Tyr
ENST00000520959.5:c.85G>T ENSP00000428496.1:p.Asp29Tyr
ENST00000522701.5:c.313G>T ENSP00000428557.1:p.Asp105Tyr
ENST00000524029.5:c.313G>T ENSP00000428237.1:p.Asp105Tyr
NM_000237.2:c.313G>T NP_000228.1:p.Asp105Tyr
NM_000237.3:c.313G>T MANE Select NP_000228.1:p.Asp105Tyr