Canonical Allele Identifier: CA1769111706
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19961888G= , CM000670.2:g.19961888G= GRCh38
NC_000008.10:g.19819399G= , CM000670.1:g.19819399G= GRCh37
NC_000008.9:g.19863679G= NCBI36
NG_008855.1:g.27818G=
NG_008855.2:g.65172G=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.1323-227G= MANE Select ENSP00000497642.1:n.1323-227G=
ENST00000650478.1:c.263-227G= ENSP00000497560.1:n.263-227G=
ENST00000311322.8:c.1323-227G= ENSP00000309757.6:n.1323-227G=
NM_000237.2:c.1323-227G= NP_000228.1:n.1323-227G=
NM_000237.3:c.1323-227G= MANE Select NP_000228.1:n.1323-227G=