Canonical Allele Identifier: CA1769098190
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19952061T= , CM000670.2:g.19952061T= GRCh38
NC_000008.10:g.19809572T= , CM000670.1:g.19809572T= GRCh37
NC_000008.9:g.19853852T= NCBI36
NG_008855.1:g.17991T=
NG_008855.2:g.55345T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.429+113T= MANE Select ENSP00000497642.1:n.429+113T=
ENST00000311322.8:c.429+113T= ENSP00000309757.6:n.429+113T=
ENST00000520959.5:c.201+113T= ENSP00000428496.1:n.201+113T=
NM_000237.2:c.429+113T= NP_000228.1:n.429+113T=
NM_000237.3:c.429+113T= MANE Select NP_000228.1:n.429+113T=