Canonical Allele Identifier: CA1769098244
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19952089T= , CM000670.2:g.19952089T= GRCh38
NC_000008.10:g.19809600T= , CM000670.1:g.19809600T= GRCh37
NC_000008.9:g.19853880T= NCBI36
NG_008855.1:g.18019T=
NG_008855.2:g.55373T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.429+141T= MANE Select ENSP00000497642.1:n.429+141T=
ENST00000311322.8:c.429+141T= ENSP00000309757.6:n.429+141T=
ENST00000520959.5:c.201+141T= ENSP00000428496.1:n.201+141T=
NM_000237.2:c.429+141T= NP_000228.1:n.429+141T=
NM_000237.3:c.429+141T= MANE Select NP_000228.1:n.429+141T=